-
Medical Devices
-
Accredited Persons Inspection Program - Guidance
- Requests for Inspection by an Accredited Person Under the Inspection by Accredited Persons Program Authorized by Section 201 of the Medical Device User Fee and Modernization Act of 2002 - Guidance for Industry, FDA Staff, and FDA-Accredited Third-Parties
- Implementation of the Inspection by Accredited Persons Program Under The Medical Device User Fee and Modernization Act of 2002; Accreditation Criteria, October 4, 2004
-
-

