01836nam 2200421Ia 450 991069665100332120080609161605.0(CKB)5470000002380352(OCoLC)231423476(EXLCZ)99547000000238035220080609d2008 ua 0engurmn|||||||||txtrdacontentcrdamediacrrdacarrierMedical devices[electronic resource] FDA faces challenges in conducting inspections of foreign 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,[2008]22 pages digital, PDF fileTestimony ;GAO-08-780 TTitle from title screen (viewed on June 5, 2008)."For release ... May 14, 2008."Paper version available from: U.S. Govt. Accountability Office, 441 G St., NW, Rm. LM, Washington, D.C. 20548.Includes bibliographical references.Medical devices Medical instruments and apparatusSafety regulationsUnited StatesMedical instruments and apparatus industryInspectionMedical instruments and apparatusSafety regulationsMedical instruments and apparatus industryInspection.Crosse Marcia1380679United States.Congress.House.Committee on Energy and Commerce.Subcommittee on Health.United States.Government Accountability Office.GPOGPOBOOK9910696651003321Medical devices3495374UNINA