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 ...