Guidance for industry, FDA staff, and FDA-accredited third parties
Manufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA)
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Contributions
- Center for Biologics Evaluation and Research (U.S.) - Contributor
Publication
2009 - U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Rockville, Md., Maryland
Language
English
Word Count
2,500 words, Guess
Page Count
10 pages
Physical Format
Electronic resource
Identifiers
- OCLC Control Number794684490
- Open LibraryOL43959378M
Alternate Titles
- Guidance for industry, Food and Drug Administration staff, and Food and Drug Administration accredited third parties.
- Manufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA)
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