FDA Inspection 1229826 — VA Medical Center-St. Louis, Human Studies Subcommittee IRB

VA Medical Center-St. Louis, Human Studies Subcommittee IRB — FEI 1937251

The FDA completed an inspection of VA Medical Center-St. Louis, Human Studies Subcommittee IRB on Feb 7, 2024 in Saint Louis, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.