Medical devices shortcomings in FDA's premarket review, postmarket surveillance, and inspections of device manufacturing establishments : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives /

Medical devices shortcomings in FDA's premarket review, postmarket surveillance, and inspections of device manufacturing establishments : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives /

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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: Electronic eBook
Language:English
Published: [Washington, D.C.] : U.S. Govt. Accountability Office, [2009]
Notes:Title from title screen (GAO, viewed July 22, 2009).
"For release ... June 18, 2009."
Description:1 online resource (18 p.) : ill.
Series:Testimony ; GAO-09-370T
Subjects:
United States. > Food and Drug Administration > Rules and practice.
Medical instruments and apparatus industry > United States.
Medical instruments and apparatus > Inspection > United States.
Risk assessment > Government policy > United States.
Online Access:http://purl.access.gpo.gov/GPO/LPS114584
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