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FDA Guidance for Industry, FDA Staff, and October 4, 2004 FDA, regulated industry, and Division of Small Third Parties; Implementation of the third parties, Manufacturers, Inspection by Accredited Persons International and Program Under the Medical De

Origin/Publisher:

FDA

Document Type:
FDA-Guidance
Content:
The purpose of the guideline is intend to implement new section of the act by accrediting third parties to conduct inspedctions of eligible manufacturers of Class II and III medical devices

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