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What to do if you get a FDA 483 Warning Letter - Webinar By GlobalCompliancePanel

29 March 2012, Wilmington, United States


Introduction
Audits by the FDA are perhaps the most intimidating of all events at a regulated facility. Each year, the FDA conducts several thousand audits, approximately half of which lead to findings that result in Form 483s.

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OnlineTraining

OnlineTraining, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States

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GlobalCompliancePanel
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OnlineTraining, 1000 N West Street Suite,, Suite 1200, Wilmington, 19801, United States of America
8004479407
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