FDA inspection
Biomat USA Inc.: FDA inspection ending Sep 23, 2014
FDA inspection 898683 · Voluntary Action Indicated (VAI) · Saint Paul, MN
Key facts
| Inspection ID | 898683 |
|---|---|
| Firm | Biomat USA Inc. |
| FEI number | 3007299028 |
| Address | 1695 Robert St S |
| City | Saint Paul |
| State | MN |
| ZIP | 55118 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Sep 23, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 1–9 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