FDA inspection
Protek Medical Products Inc: FDA inspection ending Jul 21, 2009
FDA inspection 598379 · No Action Indicated (NAI) · Coralville, IA
Key facts
| Inspection ID | 598379 |
|---|---|
| Firm | Protek Medical Products Inc |
| FEI number | 3001701594 |
| Address | 4125 Westcor Ct |
| City | Coralville |
| State | IA |
| ZIP | 52241 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jul 21, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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