You are on page 1of 37

288405382.

xlsx

Audit Contract VDA 6.3-2010

Client: (e.g. management, person responsible for the product, person responsible for th

Audited Party: (e.g. internal department, supplier)

Reason for Audit:

Audit Objective:

Audit Variant:
Internal Audit

Potential Analysis

External Audit

Special Audit

Internal Audit

external

Audit Location:

Audit Team:
Lead Auditor:
Auditors:

Process Specialist(s):

Audit Extent:
Processes:
Manufacturing
Locations:

Products:
Interfaces:

Outside Processes:

Audit Date
Desired Date:
Audit period:

Shifts:

Date of Contract

Essential Documents (test/inspections regulations, contracts, important agreements, cost stipulatio

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 1 of 37

288405382.xlsx

History (complaints, rejects, delivery performance, project status)

Remarks (background information)

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 2 of 37

288405382.xlsx

erson responsible for the audit programme)

Potential Analysis
Special Audit

nt agreements, cost stipulations, etc.)

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 3 of 37

288405382.xlsx

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 4 of 37

288405382.xlsx

VDA 6.3-2010 Audit Report: Assessment of Quality Capability


Supplier:

Client:

Supplier No.:
Location:

Reason for contract:

Assessment
index

Process/Product

Achieved

Overall Process P2 to P7

EG

nb

before SOP

ED

nb

after SOP

EP

nb

Product group 1

EPN

nb

Product group 2

EPN

nb

Product group 3

EPN

nb

Product group 4

EPN

nb

Product group 5

EPN

nb

Classified

Findings / requirements
Highlights

Product Group*

Areas of improvement

* Values automatically taken from Assessment Matrix


Classification scale: A: 90-100% (Q-capable); B: >= 80 <90% (conditionally Q-capable); C: <80% (not Q-capable)

Audit history / Certificates


Audit Basis

Date

Participants:

Set up: Rita Demmeler-Wirth

Carried out

Result

Distribution to:

Version: 2.9/10.04.2012

Page 5 of 37

288405382.xlsx
Timing for improvement plan:
For actions see 'Improvement program' and/or 'Immediate

Lead Auditor

Set up: Rita Demmeler-Wirth

Co-Auditor

Version: 2.9/10.04.2012

Page 6 of 37

288405382.xlsx

ability
Date:
Contract No.:

indings / requirements

ghlights

reas of improvement

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 7 of 37

288405382.xlsx

ming for improvement plan:


actions see 'Improvement program' and/or 'Immediate actions'

signed for Organisation

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 8 of 37

288405382.xlsx

Explanations
Supplier:

Client:

The improvement program was discussed in the final meeting on site and handed over as a draft.. The audited Organization is asked to define sustainable corrective actions
implement them rapidly.
We point out that within the audit the processes only can be checked randomly. Other weak points and / or potentials for improvement may be possible.
It is the responsibility of the audited parties to expand the investigation and necessary measures to similar areas / issues.

Participants:
Set up: Rita Demmeler-Wirth

Auditor:
Version: 2.9/10.04.2012

Page 9 of 37

288405382.xlsx

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 10 of 37

288405382.xlsx

Date:

sustainable corrective actions for the identified weak points and to

e possible.

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 11 of 37

288405382.xlsx

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 12 of 37

288405382.xlsx

VDA 6.3-2010 Audit Report: Assessment of Quality Capability


Supplier:

Client:

Assessment Elements / Process Stages

Assessment after Process Analysi


Target

Minimum requirement
per assessment element

80

60

70

80

90

90

100

Grade of fulfilment

Assessment elements /
Process stages

Assignment to
Product group

Project Management

preaudit

actual

P2

nb

P3

nb

P4

nb

P5

nb

P6

nb

P7

nb

Process Name 1

E1

nb

Process Name 2

E2

nb

Process Name 3

E3

nb

Process Name 4

E4

nb

Process Name 5

E5

nb

Process Name 6

E6

nb

Planning Product/Process

Product group 5

Product group 4

Product group 3

Product group 2

Product group 1

Carrying out Product/Process


Supplier Management
Process Analysis
Serial production
Customer Satisfaction

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 13 of 37

288405382.xlsx

Process Name 7

E7

nb

Process Name 8

E8

nb

Process Name 9

E9

nb

Process Name 10

E 10

nb
Comment:

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 14 of 37

288405382.xlsx

pability
Date:
Assessment after Process Analysis

(mean value, process stage E 1 - n) and


generic baseline
Target
Minimum requirement
80
per assessment element
60

70

80

90

90

100

Grade of fulfilment

Assessment elements /
Process stages

pre
audit

actual

Process input
EU 1

nb

EU 2

nb

EU 3

nb

EU 4

nb

EU 5

nb

EU 6

nb

EU 7

nb

Process responsibility

PR

nb

Target orientation

TO

nb

Communication

CO

nb

Risk orientation

RI

nb

Process sequence
Personnel support
Material resources
Process effectiveness level
Process result
Transport / parts handling
/ storage

Generic Baseline

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 15 of 37

288405382.xlsx

Overall Compliance

EG

nb

Before SOP

ED

nb

After SOP

EP

nb

Please input values Pre-Audit yourself


Values of actual audit will be automatically entered

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 16 of 37

288405382.xlsx

VDA 6.3-2010 Assessment Matrix including Product Groups

Notes:

Supplier:

Client:

Date:

Generic Baseline

A Development
P 2 Project Management

Achievement level %

Entry: only following values are allowed

2.1

2.2*

2.3

2.4

2.5*

2.6

2.7*

nb

nb

nb

nb

nb

nb

nb

nb not assessed
10 Requirements fully satisfied
8 Requirements mainly satisfied
6 Requirements partly satisfied
4 Requirements inadequately satisfied
0 Requirements not satisfied

PM

nb

G1

G2

G3

G4

PR

TO

CO

RI

nb

nb

nb

nb

Note: Entry "n.b." = Question not answered


Note: Entry "n.a." = Question not applicable

P 3 Planning Product/Process Development


Product
3.1
3.2*

nb

nb

3.3

3.4

3.5

nb

nb

nb

Process
3.1
3.2*

EPdP

nb

nb

nb

3.3

3.4

3.5

nb

nb

nb

EPzP

nb

PP

nb

nb

nb

nb

nb

3.1.

nb Green fields for entering

P 4 Carrying out Product/Process Development


Product
4.1
4.2

nb

nb

Blue writing -> example entry

4.3

4.4

4.5*

4.6

4.7

4.8

4.9

nb

nb

nb

nb

nb

nb

nb

Process
4.1
4.2

EPdR

nb

nb

nb

4.3

4.4

4.5*

4.6

4.7

4.8

4.9

nb

nb

nb

nb

nb

nb

nb

EPzR

nb

PR

nb

nb

nb

nb

nb

nb

nb

nb

nb

Automatic Calculation of the

B Full Production

grey, blue, yellow and red fields

P 5 Supplier Management

5.1*

5.2

5.3

5.4*

5.5*

5.6

5.7

nb

nb

nb

nb

nb

nb

nb

LM

nb

nb

nb

nb

nb

P 6 Process Analysis Serial Production


1 Process Input

2 Work Content / Process Sequences

6.1.1* 6.1.2 6.1.3 6.1.4 6.1.5


Process step 1:
Process Name 1

nb

Process step 2:

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

7 Transport and Part Handling

6 Process Result / Output


6.6.1* 6.6.2

nb

nb

6.6.3

6.6.4

nb

E1

nb

nb

Generic Baseline

6.1.2

6.1.3

6.1.4

6.2.5

6.2.6

6.4.4

6.6.2

6.6.3

G1
PR

G2
TO

G3
CO

G4
RI

PR

Process Responsibility

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

TO

Target Orientation

CO

Communication

RI

Risk Orientation

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E2

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E3

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E4

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

Reasons for downgrading

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E5

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

Down-grading from A to B despite an


achievement level of EG 90%

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E6

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E7

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E8

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E9

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

E10

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

nb

6.1.2

6.1.3

6.1.4

6.2.5

6.2.6

6.4.4

6.6.2

6.6.3

nb

nb

nb

nb

nb

nb

nb

nb

> At least one process elements P2-P7 or


process stage E1-En assessed <80 %.

Process Name 7

nb

nb

nb

Process Name 8

nb

nb

nb

Process Name 9

nb

nb

nb

Process Name 10

nb

nb

nb

nb

Assessment of Sub elements of the Process analysis (mean value step 1 - n)


1.1
1.2
1.3
1.4
1.5
2.1
2.2
2.3
2.4
2.5
nb

nb

6.5.2 6.5.3* 6.5.4*

Process Name 6

Process step 10:

nb

nb

nb

Process step 9:

nb

nb

6.5.1

Process Name 5

Process step 8:

nb

nb

nb

Process step 7:

nb

nb

5 Process Effectiveness Level

6.4.4

Process Name 4

Process step 6:

nb

nb

nb

Process step 5:

nb

nb

4 Material Resources
6.4.1 6.4.2* 6.4.3

Process Name 3

Process step 4:

nb

nb

6.3.1 6.3.2* 6.3.3

Process Name 2

Process step 3:

nb

nb

3 Personnel Support

Farbcode

nb

nb

6.2.6

nb

nb

nb

EU1

nb

nb

nb

nb

nb

nb

EU2

nb

2.6
nb

nb

3.1
nb

3.2

3.3

nb

EU3

P 7 Customer Support / Customer Satisfaction / Services

nb

4.1
nb

4.2
nb

4.3
nb

EU4

nb

4.4

5.1

nb

nb

5.2
nb

EU5

nb

7.1*

7.2

7.3*

7.4

7.5

7.6

nb

nb

nb

nb

nb

nb

5.3

5.4

nb

nb

nb

Product group 2

Product group 3

Product group 4

nb

6.2
nb

EU6

6.3

6.4

nb

nb

nb

Process Steps

Product Group

EPGN [%]

Transport, Part Handling

EPN [%]
nb

before SOP

(Part A)

ED [%]

nb

Classification

EU7

Achievement level [%] for


Generic Baseline

G1

G2

G3

G4

PR

TO

CO

RI

nb

nb

nb

nb

PR

TO

Co

RI

nb

nb

nb

nb

nb

Set up: Rita Demmeler-Wirth

(Part B)

EP [%]

nb

nb

Version: 2.9/10.04.2012

> At least one process element P2-P7 or


process stage E1-En assessed <70 %.
> Level of achievement of the sub-elements of
P6 (EU1-EU7) assessed
<70 %.
0

Classification

Overall Achievement Level EG [%]:


Classified
nb

nb
after SOP

for down-grading to C despite an achievement


level of 80 %

> At least one *-question awarded with


points.

nb

nb

> At least one *-question awarded with 4


points.

> Assessments from generic baseline assessed


<70 %.

nb

nb

Overall Achievement Level EPN [%] by


Product Groups

Product group 5

Product Group

Achievement Level

PG

EK

Achievement level EPG by Product Groups Element P6[%] (mean value Ex-En)

Product group 1

6.1

> Level of achievement of the sub-elements of


P6 (EU1-EU7) assessed
<80 %.

> At least one question from process audit


awarded with 0 points.

Farbcode

nb

6.2.1* 6.2.2 6.2.3* 6.2.4* 6.2.5

Classification results (A, B, C) must be entered manually, by taking into


account the downgrading rule!

Classification

Achievement
Level EG[%]

EG 90

Quality capable

80 EG < 90

Conditionally qualitycapable

EG < 80

Not
quality-capable

Description of
Classification

Page 17 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Quest
Nr.

Client:
Question

Points

Comments / Assessment Remarks

A Development
P 2 Project Management
2.1

2.2*

2.3
2.4
2.5*

2.6

2.7*

Is the project organisation (project management)


established and are tasks & authorities specified for the
team leader and team members?
Are the resources required for the project development
planned and available and are all changes displayed?
Is there a project plan and has this been agreed with the
customer?
Is change management in the project ensured by the
project organisation?
Are the responsible personnel within the organisation
and in the customer's company involved in the change
control system?
Is there a QM plan for the project? Is this implemented
and monitored regularly for compliance?
Is there an established escalation process and is this
implemented effectively?

nb
###

nb
nb
nb
nb
nb
nb

P 3 Planning Product/Process Development


Product
3.1

Are the product-specific requirements laid down?

3.2*

Has manufacturing feasibility been assessed in a crossfunctional manner, based on the requirements which
have been determined for product & process?

3.3
3.4

3.5

Are there plans for the product and process


development?
Have the necessary resources been taken into account
for the product and process development?
Is QM planning arranged for sourcing bought-in products
and services?

nb
nb
nb
nb
nb

Process
3.1

Are the process-specific requirements laid down?

3.2*

Has manufacturing feasibility been assessed in a crossfunctional manner, based on the requirements which
have been determined for product & process?

3.3
3.4

3.5

Are there plans for the product and process


development?
Have the necessary resources been taken into account
for the product and process development?
Is QM planning arranged for sourcing bought-in products
and services?

nb
nb
nb
nb
nb

P 4 Carrying out Product/Process Development


Product
4.1

Have the Product FMEA / Process FMEA been drawn up?


Are they up-dated as the project progresses and are
corrective actions laid down?

nb

4.2

Are the stipulations arising from the plans for product


and process development put into effect?

4.3

Are the personnel resources in place and qualified?

4.4

Is the infrastructure in place and appropriate?

nb

4.5*

Based on the requirements, are the necessary evidence


and releases available for the various phases?

nb

4.8

Are the planning activities associated with sourcing


outside products and services implemented effectively?

nb

4.9

Is the transfer of the project to production controlled in


order to secure the product launch?

nb
nb

nb

Process

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 18 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

4.1

Have the Product FMEA / Process FMEA been drawn up?


Are they up-dated as the project progresses and are
corrective actions laid down?

nb

Are the stipulations arising from the plans for product


and process development put into effect?

nb

4.2

Points

4.3

Are the personnel resources in place and qualified?

4.4

Is the infrastructure in place and appropriate?

nb

4.5*

Based on the requirements, are the necessary evidence


and releases available for the various phases?

nb

4.6

Are the productions control plans used for the various


phases and are production, test and inspection
documents derived from them?
Has a pre-production run been carried out under serial
production conditions to obtain production approval /
release?
Are the planning activities associated with sourcing
outside products and services implemented effectively?

4.7

4.8

4.9

Is the transfer of the project to production controlled in


order to secure the product launch?

Comments / Assessment Remarks

nb

nb
nb
nb
nb

B Full Production
P 5 Supplier Management
Are only approved/released and quality-capable
5.1*
5.2
5.3

suppliers selected?
Are the customer's requirements taken into account in
the supply chain?
Have target agreements for delivery performance been
agreed with suppliers and put into operation?

5.4*

Are the necessary approvals/releases available for the


out-sourced products and services?

5.5*

Is the quality of the out-sourced products and services


ensured?
Are incoming goods stored appropriately?

5.6
5.7

Are personnel qualified for the various tasks and are


responsibilities defined?

nb
nb
nb
nb
nb
nb
nb

P 6 Process Analysis Serial Production


Process step 1:
1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Process Name 1

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

Set up: Rita Demmeler-Wirth

nb
nb
nb
nb
nb
nb

Version: 2.9/10.04.2012

Page 19 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Quest
Nr.

Client:
Question

Points

Comments / Assessment Remarks

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

nb
nb
nb

4 Material Resources
6.4.1
6.4.2*

6.4.3
6.4.4

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

nb
nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

6.5.4*

Are processes and products audited regularly?

nb
nb
nb
nb

6 Process Result / Output


6.6.1*
6.6.2

6.6.3

6.6.4

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?
Are the necessary records / releases carried out and
stored appropriately?

Process step 2:

nb
nb

nb

nb

Process Name 2

1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1

Are operators given responsibility and authority to


monitor the quality of product and process?

Set up: Rita Demmeler-Wirth

nb

Version: 2.9/10.04.2012

Page 20 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

6.3.2*

Are the operators able to carry out their allotted tasks


and are their qualifications kept up-to-date?

nb

6.3.3

Is there a personnel employment plan?

nb

Points

Comments / Assessment Remarks

4 Material Resources
6.4.1
6.4.2*

6.4.3
6.4.4

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

nb
nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

6.5.4*

Are processes and products audited regularly?

nb
nb
nb
nb

6 Process Result / Output


6.6.1*
6.6.2

6.6.3

6.6.4

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?
Are the necessary records / releases carried out and
stored appropriately?

Process step 3:

nb
nb

nb
nb

Process Name 3

1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

Set up: Rita Demmeler-Wirth

nb
nb
nb

Version: 2.9/10.04.2012

Page 21 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Quest
Nr.

Client:
Question

Points

Comments / Assessment Remarks

4 Material Resources
6.4.1
6.4.2*

6.4.3
6.4.4

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

nb
nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

6.5.4*

Are processes and products audited regularly?

nb
nb
nb
nb

6 Process Result / Output


6.6.1*
6.6.2

6.6.3

6.6.4

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?
Are the necessary records / releases carried out and
stored appropriately?

Process step 4:

nb
nb

nb
nb

Process Name 4

1 Process Input
6.1.1*

Has the project been transferred from development to


serial production?

6.1.2

Are the necessary quantities / production batch sizes of


incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?

6.1.3

6.1.4

6.1.5

Are the necessary identifications / records / approvals


available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

nb
nb
nb

4 Material Resources
6.4.1

How are the maintenance and overhaul of production


facilities / tools controlled?

Set up: Rita Demmeler-Wirth

nb

Version: 2.9/10.04.2012

Page 22 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

6.4.2*

Can the quality requirements be monitored effectively


with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

6.4.3
6.4.4

Points

Comments / Assessment Remarks

nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

6.5.4*

Are processes and products audited regularly?

nb
nb
nb
nb

6 Process Result / Output


6.6.1*
6.6.2

6.6.3

6.6.4

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?
Are the necessary records / releases carried out and
stored appropriately?

Process step 5:

nb
nb

nb
nb

Process Name 5

1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

nb
nb
nb

4 Material Resources
6.4.1
6.4.2*

6.4.3

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?

Set up: Rita Demmeler-Wirth

nb
nb
nb

Version: 2.9/10.04.2012

Page 23 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

6.4.4

Are tools, equipment and test/inspection facilities stored


correctly?

Points

Comments / Assessment Remarks

nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

6.5.4*

Are processes and products audited regularly?

nb
nb
nb
nb

6 Process Result / Output


6.6.1*
6.6.2

6.6.3

6.6.4

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?
Are the necessary records / releases carried out and
stored appropriately?

Process step 6:

nb
nb

nb
nb

Process Name 6

1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

nb
nb
nb

4 Material Resources
6.4.1
6.4.2*

6.4.3
6.4.4

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

nb
nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

Set up: Rita Demmeler-Wirth

nb

Version: 2.9/10.04.2012

Page 24 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

6.5.4*

Points

Are processes and products audited regularly?

Comments / Assessment Remarks

nb
nb
nb

6 Process Result / Output


6.6.1*
6.6.2

6.6.3

6.6.4

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?
Are the necessary records / releases carried out and
stored appropriately?

Process step 7:

nb
nb

nb
nb

Process Name 7

1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

nb
nb
nb

4 Material Resources
6.4.1
6.4.2*

6.4.3
6.4.4

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

nb
nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?

Set up: Rita Demmeler-Wirth

nb
nb

Version: 2.9/10.04.2012

Page 25 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

6.5.3*

In the case of deviations from product and process


requirements, are the causes analysed and the
corrective actions checked for effectiveness?

nb

Are processes and products audited regularly?

nb

6.5.4*

Points

Comments / Assessment Remarks

6 Process Result / Output


6.6.1*
6.6.2

6.6.3

6.6.4

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?
Are the necessary records / releases carried out and
stored appropriately?

Process step 8:

nb
nb

nb
nb

Process Name 8

1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

nb
nb
nb

4 Material Resources
6.4.1
6.4.2*

6.4.3
6.4.4

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

nb
nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

Set up: Rita Demmeler-Wirth

nb
nb
nb

Version: 2.9/10.04.2012

Page 26 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

6.5.4*

Are processes and products audited regularly?

Points

Comments / Assessment Remarks

nb

6 Process Result / Output


6.6.1*
6.6.2

6.6.3

6.6.4

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?
Are the necessary records / releases carried out and
stored appropriately?

Process step 9:

nb
nb

nb
nb

Process Name 9

1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

nb
nb
nb

4 Material Resources
6.4.1
6.4.2*

6.4.3
6.4.4

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

nb
nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

6.5.4*

Are processes and products audited regularly?

nb
nb
nb
nb

6 Process Result / Output


6.6.1*

Are the customer's requirements met in terms of product


and process?

Set up: Rita Demmeler-Wirth

nb

Version: 2.9/10.04.2012

Page 27 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

6.6.2

Are quantities / production batch sizes aligned with


requirements and are they forwarded to the next process
stage in a targeted manner?
Are products / components stored in an appropriate
manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?

6.6.3

6.6.4

Points

Are the necessary records / releases carried out and


stored appropriately?

Process step 10:

Comments / Assessment Remarks

nb

nb
nb

Process Name 10

1 Process Input
6.1.1*
6.1.2

6.1.3

6.1.4

6.1.5

Has the project been transferred from development to


serial production?
Are the necessary quantities / production batch sizes of
incoming materials available at the right time and at the
right place (stores; work-station)?
Are incoming materials stored appropriately and are
transport facilities / packing arrangements suitable for
the special characteristics of the incoming materials?
Are the necessary identifications / records / approvals
available and allocated appropriately to the incoming
materials?
Are changes to the product or process in the course of
serial production tracked and documented?

nb
nb

nb

nb
nb

2 Work Content / Process Sequences


6.2.1*

6.2.2
6.2.3*
6.2.4*
6.2.5
6.2.6

Are all the relevant details listed in the production and


test/inspection documents, based on the production
control plan?
Are production operations checked / approved and are
setting data logged?
Can the customer's specific product requirements be
satisfied with the production facilities used?
Are significant characteristics controlled in production?
Are scrap, rework and setting parts kept separate and
identified?
Is the flow of materials and parts secured against mixing
/ wrong items?

nb
nb
nb
nb
nb
nb

3 Personnel Support
6.3.1
6.3.2*

6.3.3

Are operators given responsibility and authority to


monitor the quality of product and process?
Are the operators able to carry out their allotted tasks
and are their qualifications kept up-to-date?
Is there a personnel employment plan?

nb
nb
nb

4 Material Resources
6.4.1
6.4.2*

6.4.3
6.4.4

How are the maintenance and overhaul of production


facilities / tools controlled?
Can the quality requirements be monitored effectively
with the test, inspection and measurement facilities
employed?
Are the work-stations and test/inspection areas suitable
for requirements?
Are tools, equipment and test/inspection facilities stored
correctly?

nb
nb
nb
nb

5 Process Effectiveness Level


6.5.1

Are target requirements set for product and process?

6.5.2

Are quality and process data logged in such a way that


they can be assessed?
In the case of deviations from product and process
requirements, are the causes analysed and the
corrective actions checked for effectiveness?

6.5.3*

6.5.4*

Are processes and products audited regularly?

nb
nb
nb
nb

6 Process Result / Output


6.6.1*
6.6.2

Are the customer's requirements met in terms of product


and process?
Are quantities / production batch sizes aligned with
requirements and are they forwarded to the next process
stage in a targeted manner?

Set up: Rita Demmeler-Wirth

nb
nb

Version: 2.9/10.04.2012

Page 28 of 37

288405382.xlsx

Questionnaire VDA 6.3-2010

Date:

Pos
.

Supplier:

Client:

Quest
Nr.

Question

6.6.3

Are products / components stored in an appropriate


manner and are transport facilities / packing
arrangements suitable for the special characteristics of
the products / components?

nb

Are the necessary records / releases carried out and


stored appropriately?

nb

6.6.4

Points

Comments / Assessment Remarks

P 7 Customer Support / Customer Satisfaction / Services


7.1*

Are the customer's requirements satisfied regarding QM


system, product (on delivery) and process?

nb

7.2
7.3*

Is customer support ensured?

nb

Is the supply of parts ensured?

nb

7.4

If there are deviations from quality requirements, are


failure analyses carried out and corrective actions
implemented effectively?

nb

7.5
7.6

Is there a process which ensures that analysis of


defective parts is carried out?
Are personnel qualified for the various tasks and are
responsibilities defined?

Set up: Rita Demmeler-Wirth

nb
nb

Version: 2.9/10.04.2012

Page 29 of 37

288405382.xlsx

Improvement Program VDA 6.3-2010

Date:
Client:

Supplier:

Pos.

To be filled by auditor

to be filled by audited party

Weaknesses, recommended actions,


findings
A Development
Quest
No.

Actions and cause analysis by the


organisation

Points

Timing

Responsibles

Effectiveness

P 2 Project Management
2.1

nb

2.2*

nb

2.3

nb

2.4

nb

2.5*

nb

2.6

nb

2.7*

nb

P 3 Planning Product/Process Development


Product
3.1

nb

3.2*

nb

3.3

nb

3.4

nb

3.5

nb

Process
3.1

nb

3.2*

nb

3.3

nb

3.4

nb

3.5

nb

P 4 Carrying out Product/Process Development


Product
4.1

nb

4.2

nb

4.3

nb

4.4

nb

4.5*

nb

4.8

nb

4.9

nb

Process
4.1

nb

4.2

nb

4.3

nb

4.4

nb

4.5*

nb

4.6

nb

4.7

nb

4.8

nb

4.9

nb

B Full Production
P 5 Supplier Management
5.1*

nb

5.2

nb

5.3

nb

5.4*

nb

5.5*

nb

5.6

nb

5.7

nb

P 6 Process Analysis Serial Production


Process step 1:
1 Process Input

Process Name 1

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

Set up: Rita Demmeler-Wirth

nb

Version: 2.9/10.04.2012

Page 30 of 37

288405382.xlsx

Pos.

To be filled by auditor
Quest
No.

to be filled by audited party

Weaknesses, recommended actions,


findings

Actions and cause analysis by the


organisation

Points

6.3.2*

nb

6.3.3

nb

Timing

Responsibles

Effectiveness

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 2:
1 Process Input

Process Name 2

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 3:
1 Process Input

Process Name 3

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 31 of 37

288405382.xlsx

Pos.

To be filled by auditor
Quest
No.

to be filled by audited party

Weaknesses, recommended actions,


findings

Actions and cause analysis by the


organisation

Points

Timing

Responsibles

Effectiveness

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 4:
1 Process Input

Process Name 4

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 5:
1 Process Input

Process Name 5

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level

6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

Set up: Rita Demmeler-Wirth

nb

Version: 2.9/10.04.2012

Page 32 of 37

288405382.xlsx

Pos.

To be filled by auditor
Quest
No.

to be filled by audited party

Weaknesses, recommended actions,


findings

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 6:
1 Process Input

Actions and cause analysis by the


organisation

Points

Timing

Responsibles

Effectiveness

Process Name 6

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 7:
1 Process Input

Process Name 7

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 8:
1 Process Input
6.1.1*

Set up: Rita Demmeler-Wirth

Process Name 8
nb

Version: 2.9/10.04.2012

Page 33 of 37

288405382.xlsx

Pos.

To be filled by auditor
Quest
No.

to be filled by audited party

Weaknesses, recommended actions,


findings

Actions and cause analysis by the


organisation

Points

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

Timing

Responsibles

Effectiveness

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 9:
1 Process Input

Process Name 9

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

Process step 10:


1 Process Input

Process Name 10

6.1.1*

nb

6.1.2

nb

6.1.3

nb

6.1.4

nb

6.1.5

nb

2 Work Content / Process Sequences


6.2.1*

nb

6.2.2

nb

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 34 of 37

288405382.xlsx

Pos.

To be filled by auditor
Quest
No.

Weaknesses, recommended actions,


findings

to be filled by audited party

Points

6.2.3*

nb

6.2.4*

nb

6.2.5

nb

6.2.6

nb

Actions and cause analysis by the


organisation

Timing

Responsibles

Effectiveness

3 Personnel Support
6.3.1

nb

6.3.2*

nb

6.3.3

nb

4 Material Resources
6.4.1

nb

6.4.2*

nb

6.4.3

nb

6.4.4

nb

5 Process Effectiveness Level


6.5.1

nb

6.5.2

nb

6.5.3*

nb

6.5.4*

nb

6 Process Result / Output


6.6.1*

nb

6.6.2

nb

6.6.3

nb

6.6.4

nb

P 7 Customer Support / Customer Satisfaction / Services


7.1*

nb

7.2

nb

7.3*

nb

7.4

nb

7.5

nb

7.6

nb

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 35 of 37

288405382.xlsx

Disclaimer:
This template is provided free of charge by ORGAImprove to be used by interested parties.
The use of this template is within the responsibility of the user and at users risk only!
ORGAimprove will not take any responsiblity or liability for any errors e.g. in calculations / evaluations!
There is no right of support or delivery of updates by ORGAimprove!
Please note: The exact requirements for each question are provided in the 'Red Book' VDA 6.3!

nderungshistorie
Version-Nr.
1.0
1.1

Kommentar
Neuerstellung
Berechnungsfehler behoben

Datum
11/1/2010
12/1/2010

Name
R. Demmeler-Wirth
R. Demmeler-Wirth

1.2

Berechnungsfehler P2 behoben
Ermglichung der Eingabe 'na' nicht anwendbar
Berechnungsfehler P7 behoben

2/10/2011

R. Demmeler-Wirth

2.0

* Rundungsfehler in %ualen Berechnungen


behoben
* P4 Feld 4.6 + 4.7 n.a., da nicht bei
Produktentwicklung nicht relevant
* Korrektur div. Formatierungen
* Feldformatierungen bei Werten, die zu
Abstufungen fhren (Orange zu B, Rot zu C)
* Verknpfung Werte Auditbericht mit
Bewertungsmatrix
* Verknpfungen Lieferent, Auftraggeber und
Datum mit Auditbericht
* Verknpfungen Fragen mit Bewertungsmatrix und
Verbesserungsprogramm
4/2/2011

R. Demmeler-Wirth

2.1

Verbesserungen in Bewertungsmatrix (5.Feld


Gesamterfllungsgrad Produktgruppe)
Formatierungen (zulassen von Zeilenhhe /
Spaltenbreite
Dropdown im Fragekatalog inkl. Farb-Formatierung 4/12/2011

R. Demmeler-Wirth

Verbesserungsprogramm & Fragenkatalog:

2.2

Spalten E & I neu formatiert (Zeilenumbruch,


Einzug horizontal links, Ausrichtung vertikal oben)
Bewertungsmatrix:
P3 & P4 Prozess neu mit Fragenkatalog verknpft
P4 Frage 4.5 auf nb und 4.7 mit Fragenkatalog
verknpft

2.3

Korrektur Berechnung Produktgruppenbewertung


berarbeitung automatische Farbcodierung
Korrektur P4 4.5-4.7 Fragekatalog 4.5 eingestellt
und 4.7 gelscht

4/29/2011

R. Demmeler-Wirth

2.4
2.5
2.6

Layoutverbesserung Bewertungsmatrix,
Korrekturen Automatische Farbe
Div. Verbesserungen und berarbeitung
Verlinkungen
Korrektur Gruppierungen
Ergebnisbersicht Vor / Nach SOP eingefgt
kleinere Korrekturen (Rahmen, Text)
Generischen Ansatz Berechnung korrigiert

5/29/2011
6/27/2011
9/27/2011

R. Demmeler-Wirth
R. Demmeler-Wirth
R. Demmeler-Wirth

2.7

Kommastelle beim generischen Ansatz zugefgt

9/27/2011

R. Demmeler-Wirth

2.8

Formatierung Generischer Ansatz (Rahmen)


Abkrzungen PR,CO,TO,RI zugefgt

3/14/2012

R. Demmeler-Wirth

2.9

Korrektur Rechtschreibfehler und bersetzungen


Korrektur Bewertung Erklrung Einstufung >= 90
= A statt >90 = A

4/10/2012

R. Demmeler-Wirth

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 36 of 37

288405382.xlsx

uations!

Set up: Rita Demmeler-Wirth

Version: 2.9/10.04.2012

Page 37 of 37

You might also like