FDA inspection
Biomat USA, Inc.: FDA inspection ending Mar 17, 2022
FDA inspection 1167592 · No Action Indicated (NAI) · Saint Louis, MO
Key facts
| Inspection ID | 1167592 |
|---|---|
| Firm | Biomat USA, Inc. |
| FEI number | 1971882 |
| Address | 5121 Delmar Blvd |
| City | Saint Louis |
| State | MO |
| ZIP | 63108 |
| Country | United States |
| Fiscal year | 2022 |
| Inspection end date | Mar 17, 2022 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data