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001 9910698838203321
005 20090521130314.0
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035   $a(EXLCZ)995470000002397485
100   $a20090521d2004      ua             0
101 0 $aeng
135   $auran|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aImplementation of the Inspection by Accredited Persons Program under the Medical Device User Fee and Modernization Act of 2002, accreditation criteria$b[electronic resource]
210  1$aRockville, MD :$cU.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health :$cCenter for Biologics Evaluation and Research,$d[2004]
215   $a31 pages $cdigital, PDF file
300   $aTitle from PDF title page (viewed on May 21, 2009).
300   $a"Document issued on: October 4, 2004".
517 1 $aGuidance for industry, FDA staff, and third parties
606   $aMedical instruments and apparatus$xGovernment policy$zUnited States
615  0$aMedical instruments and apparatus$xGovernment policy
712 02$aCenter for Devices and Radiological Health (U.S.)
712 02$aCenter for Biologics Evaluation and Research (U.S.)
801  0$bGPO
801  1$bGPO
906   $aBOOK
912   $a9910698838203321
996   $aImplementation of the Inspection by Accredited Persons Program under the Medical Device User Fee and Modernization Act of 2002, accreditation criteria$93174906
997   $aUNINA