FDA inspection
Biomat USA Inc: FDA inspection ending Dec 22, 2011
FDA inspection 760034 · Voluntary Action Indicated (VAI) · Glendale, AZ
Key facts
| Inspection ID | 760034 |
|---|---|
| Firm | Biomat USA Inc |
| FEI number | 2077878 |
| Address | 5048 W Northern Ave Ste 101 |
| City | Glendale |
| State | AZ |
| ZIP | 85301 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Dec 22, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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