01691nam 2200397Ia 450 991069648930332120080222163423.0(CKB)5470000002377945(OCoLC)197148137(EXLCZ)99547000000237794520080222d2008 ua 0engurmn|||||||||txtrdacontentcrdamediacrrdacarrierMedical devices[electronic resource] challenges for FDA in conducting manufacturer inspections : testimony before the Subcommittee on Oversight and Investigations, Committee on Energy and Commerce, House of Representatives /statement of Marcia Crosse[Washington, D.C.] :U.S. Govt. Accountability Office,[2008]26 pages digital, PDF fileTestimony ;GAO-08-428 TTitle from title screen (viewed on Feb. 20, 2008)."For release ... January 29, 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 apparatus industryUnited StatesMedical instruments and apparatus industryCrosse Marcia1380679United States.Congress.House.Committee on Energy and Commerce.Subcommittee on Oversight and Investigations.United States.Government Accountability Office.GPOGPOBOOK9910696489303321Medical devices3495374UNINA