B
BWoods
What kind of issues have you had with products that were designed and released prior to your becoming a "QS house?"
Certainly we don't need to show APQP compliance if the design cycle was completed prior to becoming QS. But what about PFMEAs, Control Plans, etc.? And once we pass the certification, how do you handle PPAPs?
We have several products that are Pre-QS. My intention is to say they are not QS and are not under the QS system. I did that previously in both QS and VDA 6.1 without a problem. But with different auditors. What do you all think? How are you handling these types of problems?
Certainly we don't need to show APQP compliance if the design cycle was completed prior to becoming QS. But what about PFMEAs, Control Plans, etc.? And once we pass the certification, how do you handle PPAPs?
We have several products that are Pre-QS. My intention is to say they are not QS and are not under the QS system. I did that previously in both QS and VDA 6.1 without a problem. But with different auditors. What do you all think? How are you handling these types of problems?