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This is a list of FOIA requests for copies of 483s and EIRs for inspections of CROs, testing labs, sponsor/monitors, IRBs and clinical investigators, which were filed with FDA under the Freedom of Information Act (FOIA). This list does not imply that a 483 or EIR has been issued, only that a request for a copy has been made by a third party. These documents - if actually available - usually must be requested anew from our RECORD-RETRIEVE Service by referencing the FDA file # (i.e., F01023190), or you can submit on your own by referencing the FDA file number. The weeks of 11/5, 12, 19, 26 and 12/3/01 were used to compile this list. To order any of these files, call our …