FDA inspection
Biomat USA Inc: FDA inspection ending Jan 28, 2011
FDA inspection 708048 · No Action Indicated (NAI) · Aurora, CO
Key facts
| Inspection ID | 708048 |
|---|---|
| Firm | Biomat USA Inc |
| FEI number | 1718620 |
| Address | 501 Sable Blvd |
| City | Aurora |
| State | CO |
| ZIP | 80011 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Jan 28, 2011 |
| 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