FDA inspection
Biomat USA, Inc: FDA inspection ending Mar 12, 2014
FDA inspection 870408 · No Action Indicated (NAI) · Tuscaloosa, AL
Key facts
| Inspection ID | 870408 |
|---|---|
| Firm | Biomat USA, Inc |
| FEI number | 1037531 |
| Address | 3201 10th Ave Ste E |
| City | Tuscaloosa |
| State | AL |
| ZIP | 35401 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Mar 12, 2014 |
| 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
- 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