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Veterans Affairs Medical Center

FDA establishment 1970687, Saint Louis, Missouri, United States. Every inspection FDA has posted for the site, with its outcome and cited regulations.

  • Inspections: 8
  • Official action indicated: 0
  • Last inspection ended: Sep 25, 2025
  • Warning letters: 0

Inspections by Fiscal Year

FY2018 to FY2027 to date; 0 classified OAI

Most Cited at This Site

Inspections citing each reference

Inspections

8 inspections, newest first
EndedProduct and areaCitationsClassification
Sep 25, 2025Biologics · Blood and Blood ProductsNone postedNo Action Indicated (NAI)
Jan 16, 2020Biologics · Blood and Blood ProductsNone postedNo Action Indicated (NAI)
Jun 7, 2018Biologics · Blood and Blood ProductsNone postedNo Action Indicated (NAI)
Dec 17, 2015Biologics · Blood and Blood Products
4 cited references
  • 21 CFR 606.140(b). Provisions to monitor lab test procedures & instruments Failure to establish adequate provisions for monitoring the accuracy and precision and performance of laboratory test procedures and instruments.
  • 21 CFR 640.11(a). General requirements - storage Failure to store and maintain the Red Blood Cells between 1 and 6 degrees Celsius immediately after processing.
  • 21 CFR 606.100(c). Thorough investigations Failure to perform a thorough investigation and make a record of the conclusions and follow-up of an unexplained discrepancy and a failure of a lot or unit to meet any of its specifications .
  • 21 CFR 606.60(a). Equipment observed, standardized, calibrated Equipment used in the storage and distribution of blood and blood components is not calibrated on a regularly scheduled basis as prescribed in the SOP Manual.
Voluntary Action Indicated (VAI)
Jan 9, 2014Biologics · Blood and Blood ProductsNone postedNo Action Indicated (NAI)
Mar 14, 2013Biologics · Blood and Blood ProductsNone postedNo Action Indicated (NAI)
Mar 31, 2011Biologics · Blood and Blood ProductsNone postedVoluntary Action Indicated (VAI)
Jun 10, 2009Biologics · Blood and Blood ProductsNone postedNo Action Indicated (NAI)

Identifiers

FEI number
1970687
FDA firm profile
Data Dashboard

An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm. FDA Data Dashboard and warning letters

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