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).

Bibliographic Details
Corporate Authors:	Center for Devices and Radiological Health (U.S.), Center for Biologics Evaluation and Research (U.S.)
Format:	Government Document eBook
Language:	English
Published:	[Rockville, Md.] : [Bethesda, Md.] : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health ; Center for Biologics Evaluation and Research, [2009]
Subjects:	Medical instruments and apparatus > Government policy > United States. United States. > Food and Drug Administration.
Online Access:	https://purl.fdlp.gov/GPO/gpo23189

Description
Item Description:	Title from PDF title screen (viewed May 24, 2012). "Document issued on March 2, 2009." "This document supersedes the document which was issued on September 15, 2005." Electronic resource.
Physical Description:	1 online resource (10 pages)