Tumbleweed Tim wrote:Anyone know if after you establish a sample size, would an inspection plan, describing what to inspect and how be a requirement for a sound system?
At places I have worked in the past usual plan was a folder with characteristics listed, sometimes by the QC person sometimes by the ME, QE, or manager.
I think the documentation should include everything necessary to disposition the inspected material. In my opinion it should describe (off the top of my head):
- the product,
- the procedure and/or test method,
- the personnel requirements,
- the quality characteristics and their classifications,
- sample size, frequency, acceptance number or decision limits.
- the definition of a lot,
- what to do with a lot when accepted and if rejected (rework, scrap, etc.),
- and what records are kept of the inspection.
I also think the decision properties of the sampling plan should be documented:
- Acceptable Quality Level (AQL)
- Rejectable Quality Level (RQL)
- Producer's Risk (Alpha)
- Consumer's Risk (Beta)
- the Operating Characteristic Curve (OC Curve)
- the within-lot standard deviation for variables plans
- the source of the sampling plan.
Seems to me if I was an auditor after asking how to get a sample size, I might want to know what you are going to inspect and how.
If I were the auditor I would be suspicious that the plan might not be a reality if I did not see that documented.