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VDA & TS 16949 Release Parts Process Comparison - Page 2


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Some Related Topic Tags (Not all threads are Tagged)
ts 16949 - automotive quality system standard, vda standards
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  Post Number #9  
Old 6th April 2006, 01:22 AM
yapijingo - 2008

 
 
Total Posts: 21
No, Just one project have many parts, Some parts is release by our Germany company, Some is release by our Chinese company .
Our line will set up at Germany then transfer to China.
As project coordinator, I need push all guy release parts on time, But Germany side insist need get trial run result then release it, No special explain.Thanks for your data and answer.

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  Post Number #10  
Old 6th April 2006, 01:34 AM
Howard Atkins's Avatar
Howard Atkins

 
 
Total Posts: 2,957
I trust that it has helped
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  Post Number #11  
Old 15th September 2016, 09:43 AM
Moncia's Avatar
Moncia

 
 
Total Posts: 133
Please Help! Re: VDA & TS 16949 Release Parts Process Comparison

Hello

i have a problem i cannot figure out and it is related to this discussion

I am hoping someone can help me

our little company is not TS certified but we started to supply to some automotive customers so we occasionally are asked to do PPAP
two months ago - we had our first and only VDA audit

we had explained to the auditor we are only ISO 9001 certified which he said its ok - he would only audit our QM system

then the audit happened - wasnt that bad

but the auditor left me with OFI and one - i have no idea how to close

we had closed all other points but i am holding closing all the action plan and reply to the customer because i have no clue what he want us to do

quoted point from his report - Releases of the suppliers should be implemented, a monitor including the status of each supplier has to be done.

i have tried to ask his advice but all he gave me was more requirements but no explanation what to do to be compliant

quoted here his reply to my email -
According to the ISO/TS and the VDA standard, every part for automotive have to be approved with the supplier.
For each approval, you have to send a release (Could be conditional release if there are some deviations)

You can create a system to validate the process and the products with the suppliers. Like a PPAP system with a final release at the end of the process.

can someone please tell me what we have to do - send me some example ???
i have no idea

please
  Post Number #12  
Old 21st September 2016, 10:16 AM
delanga25

 
 
Total Posts: 1
Re: VDA & TS 16949 Release Parts Process Comparison

Can you provide more details.
Do you currently approve your Suppliers via PPAP submission?
How do you Approve the use of the parts that are being supply to you?
  Post Number #13  
Old 22nd September 2016, 03:26 AM
Great Scotch

 
 
Total Posts: 7
Re: VDA & TS 16949 Release Parts Process Comparison

Quote:
In Reply to Parent Post by Moncia View Post

Hello

i have a problem i cannot figure out and it is related to this discussion

I am hoping someone can help me

our little company is not TS certified but we started to supply to some automotive customers so we occasionally are asked to do PPAP
two months ago - we had our first and only VDA audit

we had explained to the auditor we are only ISO 9001 certified which he said its ok - he would only audit our QM system

then the audit happened - wasnt that bad

but the auditor left me with OFI and one - i have no idea how to close

we had closed all other points but i am holding closing all the action plan and reply to the customer because i have no clue what he want us to do

quoted point from his report - Releases of the suppliers should be implemented, a monitor including the status of each supplier has to be done.

i have tried to ask his advice but all he gave me was more requirements but no explanation what to do to be compliant

quoted here his reply to my email -
According to the ISO/TS and the VDA standard, every part for automotive have to be approved with the supplier.
For each approval, you have to send a release (Could be conditional release if there are some deviations)

You can create a system to validate the process and the products with the suppliers. Like a PPAP system with a final release at the end of the process.

can someone please tell me what we have to do - send me some example ???
i have no idea

please
Was it a VDA6.3 process audit?
If yes...
Which question did you get?
How many points?
What were the remarks?
Which process were you audited?
  Post Number #14  
Old 30th September 2016, 06:00 AM
Chaithanyia

 
 
Total Posts: 4
What is 'D' Characteristics in VDA 6.3?

Hi,

I came across a question during VDA6.3 Audit P7.1 which asked for the Audit Plan of 'D' Characteristics

Can any one guide me to understand what is 'D' Characteristics in VDA 6.3?

Thanks in advance.
  Post Number #15  
Old 2nd November 2016, 03:09 AM
Great Scotch

 
 
Total Posts: 7
Re: What is 'D' Characteristics in VDA 6.3?

Quote:
In Reply to Parent Post by Chaithanyia View Post

Hi,

I came across a question during VDA6.3 Audit P7.1 which asked for the Audit Plan of 'D' Characteristics

Can any one guide me to understand what is 'D' Characteristics in VDA 6.3?

Thanks in advance.
VDA 6.3, Pos. 7.1
D characteristics are characteristics requiring special verification, documentation all related processes for these to facilitate.
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