Medical devices : FDA faces challenges in conducting inspections of foreign manufacturing establishments : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives /

Bibliographic Details
Main Author:	Crosse, Marcia
Corporate Authors:	United States. Congress. House. Committee on Energy and Commerce. Subcommittee on Health, United States. Government Accountability Office
Format:	Government Document eBook
Language:	English
Published:	[Washington, D.C.] : U.S. Govt. Accountability Office, [2008]
Series:	Testimony ; GAO-08-780 T.
Subjects:	United States. > Food and Drug Administration. Medical instruments and apparatus > Safety regulations > United States. Medical instruments and apparatus industry > Inspection.
Online Access:	https://purl.fdlp.gov/GPO/LPS95065

Description
Item Description:	Title from title screen (viewed on June 5, 2008). "For release ... May 14, 2008." Paper version available from: U.S. Govt. Accountability Office, 441 G St., NW, Rm. LM, Washington, D.C. 20548. Electronic resource.
Physical Description:	22 pages : digital, PDF file.
Format:	Mode of access: Internet from GPO Access web site. Address as of 6/5/08: http://frwebgate.access.gpo.gov/cgi-bin/getdoc.cgi?dbname=gao&docid=f:d08780t.pdf ; current access available via PURL.
Bibliography:	Includes bibliographical references.