FDA inspection
Smith & Nephew, Inc. Advanced Surgical Devices Division: FDA inspection ending Jun 11, 2013
FDA inspection 834988 · Voluntary Action Indicated (VAI) · Oklahoma City, OK
Key facts
| Inspection ID | 834988 |
|---|---|
| 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 | 2013 |
| Inspection end date | Jun 11, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| 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