FDA inspection
Smith & Nephew Orthopaedics Ltd. (Aurora): FDA inspection ending Mar 27, 2008
FDA inspection 516495 · No Action Indicated (NAI) · Leamington Spa
Key facts
| Inspection ID | 516495 |
|---|---|
| Firm | Smith & Nephew Orthopaedics Ltd. (Aurora) |
| FEI number | 3005975929 |
| Address | Aurora, Spa Park, Harrison Way |
| City | Leamington Spa |
| Fiscal year | 2008 |
| Inspection end date | Mar 27, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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