01599nam 2200349Ia 450 991069883820332120090521130314.0(CKB)5470000002397485(OCoLC)334756488(EXLCZ)99547000000239748520090521d2004 ua 0enguran|||||||||txtrdacontentcrdamediacrrdacarrierImplementation of the Inspection by Accredited Persons Program under the Medical Device User Fee and Modernization Act of 2002, accreditation criteria[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,[2004]31 pages digital, PDF fileTitle from PDF title page (viewed on May 21, 2009)."Document issued on: October 4, 2004".Guidance for industry, FDA staff, and third partiesMedical instruments and apparatusGovernment policyUnited StatesMedical instruments and apparatusGovernment policyCenter for Devices and Radiological Health (U.S.)Center for Biologics Evaluation and Research (U.S.)GPOGPOBOOK9910698838203321Implementation of the Inspection by Accredited Persons Program under the Medical Device User Fee and Modernization Act of 2002, accreditation criteria3174906UNINA