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100   $a20080609d2008      ua             0
101 0 $aeng
135   $aurmn|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 10$aMedical devices$b[electronic resource] $eFDA faces challenges in conducting inspections of foreign manufacturing establishments : testimony before the Subcommittee on Health, Committee on Energy and Commerce, House of Representatives /$fstatement of Marcia Crosse
210  1$a[Washington, D.C.] :$cU.S. Govt. Accountability Office,$d[2008]
215   $a22 pages $cdigital, PDF file
225 1 $aTestimony ;$vGAO-08-780 T
300   $aTitle from title screen (viewed on June 5, 2008).
300   $a"For release ... May 14, 2008."
300   $aPaper version available from: U.S. Govt. Accountability Office, 441 G St., NW, Rm. LM, Washington, D.C. 20548.
320   $aIncludes bibliographical references.
517   $aMedical devices 
606   $aMedical instruments and apparatus$xSafety regulations$zUnited States
606   $aMedical instruments and apparatus industry$xInspection
615  0$aMedical instruments and apparatus$xSafety regulations
615  0$aMedical instruments and apparatus industry$xInspection.
700   $aCrosse$b Marcia$01380679
712 02$aUnited States.$bCongress.$bHouse.$bCommittee on Energy and Commerce.$bSubcommittee on Health.
712 02$aUnited States.$bGovernment Accountability Office.
801  0$bGPO
801  1$bGPO
906   $aBOOK
912   $a9910696651003321
996   $aMedical devices$93495374
997   $aUNINA