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005 20090519154157.0
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135   $auran|||||||||
181   $ctxt$2rdacontent
182   $cc$2rdamedia
183   $acr$2rdacarrier
200 00$aRequests for inspection by an accredited person under the Inspection by Accredited Persons Program authorized by Section 201 of the Medical Device User Fee and Modernization Act of 2002$b[electronic resource]
210  1$a[Rockville, 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[2005]
215   $a11 pages $cdigital, PDF file
300   $aTitle from PDF title page (viewed on May 19, 2009).
300   $a"Document issued on: September 15, 2005".
517 1 $aGuidance for industry, FDA staff, and FDA-accredited third parties
606   $aMedical instruments and apparatus$xInspection$zUnited States
615  0$aMedical instruments and apparatus$xInspection
712 02$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   $a9910698843303321
996   $aRequests for inspection by an accredited person under the Inspection by Accredited Persons Program authorized by Section 201 of the Medical Device User Fee and Modernization Act of 2002$93174957
997   $aUNINA