Hi we are going to have an audit 16949 certification and we have an issue about traceability.
Firstly I want to explain our structure and situation. We have 2 types of product. First one for aftermarket which is complex and has a multiple components. and second one is for OE , not complex, 1 or 2 components it has. We assure traceability on OE parts both with ERP and physical from packaging to supplier since it has 1 or 2 component.
But we cant sustain traceability both ERP and physical on aftermarket products. We assure only with ERP. Because aftermarket products have multi components and big lots, so they are mixing each other at some level.
So my question is, do auditors write a nonconformity according this situatin, if they do woul it be a major or minor?
Also Do you have a suggestion to ensure traceability on Aftermarket multicomponents product with a easy way?
Firstly I want to explain our structure and situation. We have 2 types of product. First one for aftermarket which is complex and has a multiple components. and second one is for OE , not complex, 1 or 2 components it has. We assure traceability on OE parts both with ERP and physical from packaging to supplier since it has 1 or 2 component.
But we cant sustain traceability both ERP and physical on aftermarket products. We assure only with ERP. Because aftermarket products have multi components and big lots, so they are mixing each other at some level.
So my question is, do auditors write a nonconformity according this situatin, if they do woul it be a major or minor?
Also Do you have a suggestion to ensure traceability on Aftermarket multicomponents product with a easy way?