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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). Preview this item
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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).

Author: Center for Devices and Radiological Health (U.S.); Center for Biologics Evaluation and Research (U.S.)
Publisher: [Rockville, Md.] : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health ; [Bethesda, Md.] : Center for Biologics Evaluation and Research, [2009]
Edition/Format:   eBook : Document : National government publication : English
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Material Type: Document, Government publication, National government publication, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: Center for Devices and Radiological Health (U.S.); Center for Biologics Evaluation and Research (U.S.)
OCLC Number: 794684490
Notes: Title from PDF title screen (viewed May 24, 2012).
"Document issued on March 2, 2009."
"This document supercedes the document which was issued on September 15, 2005."
Description: 1 online resource (10 pages)
Other 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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