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Zdrowie i gospodarka · 04/10/2004

FDA Updates Accreditation Criteria for Medical Device Inspections

The Food and Drug Administration (FDA) has revised its criteria for accrediting persons to conduct inspections of eligible device manufacturers under the Medical Device User Fee and Modernization Act of 2002 (MDUFMA), and made the new guidance document available for public review.

Source: Federal Register — Food and Drug AdministrationOpen original release →