FDA inspection
Biomat USA, Inc.: FDA inspection ending Oct 17, 2016
FDA inspection 989350 · No Action Indicated (NAI) · Portland, OR
Key facts
| Inspection ID | 989350 |
|---|---|
| Firm | Biomat USA, Inc. |
| FEI number | 3005600120 |
| Address | 8033 SE Holgate Blvd |
| City | Portland |
| State | OR |
| ZIP | 97206 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Oct 17, 2016 |
| 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