FDA inspection
Smith & Nephew, Inc. Advanced Surgical Devices Division: FDA inspection ending Jul 31, 2009
FDA inspection 601510 · Voluntary Action Indicated (VAI) · Oklahoma City, OK
Key facts
| Inspection ID | 601510 |
|---|---|
| Firm | Smith & Nephew, Inc. Advanced Surgical Devices Division |
| FEI number | 1643264 |
| Address | 76 S Meridian Ave |
| City | Oklahoma City |
| State | OK |
| ZIP | 73107 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jul 31, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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