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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 / statement of Marcia Crosse.
- Format:
- Book
- Government document
- Author/Creator:
- Crosse, Marcia
- Series:
- Testimony ; GAO-09-370T.
- Testimony ; GAO-09-370T
- Language:
- English
- Subjects (All):
- United States. Food and Drug Administration--Rules and practice.
- United States.
- United States. Food and Drug Administration.
- Medical instruments and apparatus industry--United States.
- Medical instruments and apparatus industry.
- Medical instruments and apparatus--Inspection--United States.
- Medical instruments and apparatus.
- Risk assessment--Government policy--United States.
- Risk assessment.
- Medical instruments and apparatus--Inspection.
- Risk assessment--Government policy.
- Genre:
- Rules and practice.
- Rules
- Physical Description:
- 1 online resource (18 pages) : illustrations.
- Other Title:
- Shortcomings in FDA's premarket review, postmarket surveillance, and inspections of device manufacturing establishments
- Place of Publication:
- [Washington, D.C.] : U.S. Govt. Accountability Office, [2009]
- Notes:
- Title from title screen (GAO, viewed July 22, 2009).
- "For release ... June 18, 2009."
- Includes bibliographical references.
- OCLC:
- 430340142
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