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This 30-page checklist covers
both 13485:2003 and FDA QSR (21 CFR 820) compliance. In addition
to general topics the checklist also includes specific, practical
questions and tips with auditing techniques. This is especially
helpful for inexperienced auditors and for auditor training.
To download demo (MS Word file), click on appropriate picture or link. Your browser will
do the rest.
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