FDA inspection
Oscor Inc.: FDA inspection ending Dec 12, 2008
FDA inspection 551858 · Voluntary Action Indicated (VAI) · Palm Harbor, FL
Key facts
| Inspection ID | 551858 |
|---|---|
| Firm | Oscor Inc. |
| FEI number | 1035166 |
| Address | 3816 Desoto Blvd |
| City | Palm Harbor |
| State | FL |
| ZIP | 34683 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Dec 12, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes 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