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 /

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, [2009]
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:	https://purl.fdlp.gov/GPO/LPS114584

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