01852nam 2200433 a 450 991069906900332120090813112543.0(CKB)5470000002399194(OCoLC)430340142(EXLCZ)99547000000239919420090813d2009 ua 0engurmn|||||||||txtrdacontentcrdamediacrrdacarrierMedical devices[electronic resource] 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[Washington, D.C.] :U.S. Govt. Accountability Office,[2009]1 online resource (18 pages) illustrationsTestimony ;GAO-09-370TTitle from title screen (GAO, viewed July 22, 2009)."For release ... June 18, 2009."Includes bibliographical references.Medical devices Medical instruments and apparatus industryUnited StatesMedical instruments and apparatusInspectionUnited StatesRisk assessmentGovernment policyUnited StatesMedical instruments and apparatus industryMedical instruments and apparatusInspectionRisk assessmentGovernment policyCrosse Marcia1380679United States.Congress.House.Committee on Energy and Commerce.Subcommittee on Health.United States.Government Accountability Office.GPOGPOBOOK9910699069003321Medical devices3495374UNINA