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 /
[Washington, D.C.] :
U.S. Govt. Accountability Office,
|Notes:||Title from title screen (GAO, viewed July 22, 2009).|
"For release ... June 18, 2009."
|Description:||1 online resource (18 p.) : ill.|
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