FDA inspection
Generic Medical Devices, Inc.: FDA inspection ending Sep 9, 2010
FDA inspection 680230 · Official Action Indicated (OAI) · Gig Harbor, WA
Key facts
| Inspection ID | 680230 |
|---|---|
| Firm | Generic Medical Devices, Inc. |
| FEI number | 3006142121 |
| Address | 5727 Baker Way NW Ste 201 |
| City | Gig Harbor |
| State | WA |
| ZIP | 98332 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Sep 9, 2010 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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