01675nam 2200349Ia 450 991069884330332120090519154157.0(CKB)5470000002397433(OCoLC)326879156(EXLCZ)99547000000239743320090519d2004 ua 0enguran|||||||||txtrdacontentcrdamediacrrdacarrierRequests 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[electronic resource][Rockville, MD] :U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health :Center for Biologics Evaluation and Research,[2005]11 pages digital, PDF fileTitle from PDF title page (viewed on May 19, 2009)."Document issued on: September 15, 2005".Guidance for industry, FDA staff, and FDA-accredited third partiesMedical instruments and apparatusInspectionUnited StatesMedical instruments and apparatusInspectionCenter for Devices and Radiological Health (U.S.)Center for Biologics Evaluation and Research (U.S.)GPOGPOBOOK9910698843303321Requests 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 20023174957UNINA