FDA establishment 1937473, Saint Louis, Missouri, United States. Every inspection FDA has posted for the site, with its outcome and cited regulations.
FY2018 to FY2027 to date; 0 classified OAI
A hatched bar is a year that is not over, so its count covers only part of the year.
Inspections citing each reference
| Nov 20, 2025 | Biologics · Blood and Blood Products | 2 cited references
| Voluntary Action Indicated (VAI) |
| Nov 10, 2022 | Biologics · Vaccines and Allergenic ProductsBiologics · Blood and Blood Products | None posted | No Action Indicated (NAI) |
| Aug 28, 2018 | Biologics · Human Cellular, Tissue, and Gene TherapiesBiologics · Blood and Blood Products | None posted | No Action Indicated (NAI) |
| Jan 26, 2015 | Biologics · Blood and Blood ProductsBiologics · Human Cellular, Tissue, and Gene Therapies | None posted | No Action Indicated (NAI) |
| Dec 10, 2012 | Biologics · Blood and Blood Products | None posted | No Action Indicated (NAI) |
| Jan 19, 2011 | Biologics · Blood and Blood Products | None posted | No Action Indicated (NAI) |
| Jun 11, 2009 | Biologics · Blood and Blood Products | None posted | No Action Indicated (NAI) |
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. Recalls come from FDA's enforcement reports (iRES), one row per recall even when it covers many lots. 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, warning letters and enforcement reports
Saint Louis, Missouri, United States. Every inspection FDA has posted for the site, with its outcome and cited regulations.