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 # (e.g., F01023190), or you can submit on your own by referencing the FDA file number. (The week of July 23, 2007, was used to compile this list.) To order any of these files, call our RECORD-RETRIEVE Service at (703) 779-8777, or e-mail at SERVICE@FDAINFO.COM
BiMo inspection FOIA log.(Brief article)
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