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.

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 : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health : Center for Biologics Evaluation and Research, [2005]
Subjects:	Medical instruments and apparatus > Inspection > United States.
Online Access:	https://purl.fdlp.gov/GPO/LPS112835

Description
Item Description:	Title from PDF title page (viewed on May 19, 2009). "Document issued on: September 15, 2005". Electronic resource.
Physical Description:	11 pages : digital, PDF file.
Format:	Mode of access: Internet at the FDA CBER web site. Address as of 5/19/09: http://www.fda.gov/cdrh/comp/guidance/1532.pdf ; current access is available via PURL.