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 |
 |
 |
Back to Accredited Persons Inspection Program
Updated October
6, 2005

CDRH Home Page | CDRH A-Z Index | Contact CDRH | Accessibility | Disclaimer FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | HHS Home Page
Center for Devices and Radiological Health / CDRH |