Monya1
5th November 2002, 08:22 PM
Our company is currently developing processes and subsequent documentation for ISO9000 / 2000 (9002) and I am needing clarification about in-process inspection data collection requirements. We are a sheet metal fabrication facility.
When the operator performs in-process inspections, based on critical dimensions as defined by engineering and specified intervals, does the operator have to document the readings they take or can they simply check OK if the measurments conform to the required tolerances? If the dimensions fail inspection then we would have the operator document their readings and what they did to get the process under control.
On first piece we also have the QA Tech inspect the part and sign the Shop Traveler for each operation. QA tech does not record his readings unless we are required to do so by the customer on a First Article Inspection form.
Hope this is not too lengthy or confusing. Thanks for any help you can offer.
Mona
When the operator performs in-process inspections, based on critical dimensions as defined by engineering and specified intervals, does the operator have to document the readings they take or can they simply check OK if the measurments conform to the required tolerances? If the dimensions fail inspection then we would have the operator document their readings and what they did to get the process under control.
On first piece we also have the QA Tech inspect the part and sign the Shop Traveler for each operation. QA tech does not record his readings unless we are required to do so by the customer on a First Article Inspection form.
Hope this is not too lengthy or confusing. Thanks for any help you can offer.
Mona





