FDA inspection
Smith & Nephew Orthopaedics GmbH: FDA inspection ending Jul 22, 2010
FDA inspection 681881 · Official Action Indicated (OAI) · Tuttlingen
Key facts
| Inspection ID | 681881 |
|---|---|
| Firm | Smith & Nephew Orthopaedics GmbH |
| FEI number | 3002465897 |
| Address | Alemannenstr. 14 |
| City | Tuttlingen |
| Country | Germany |
| Fiscal year | 2010 |
| Inspection end date | Jul 22, 2010 |
| Classification | Official Action Indicated (OAI) |
| Project area | Project Evaluation: Devices |
| Product type | Devices |
| Warning letter | 147052 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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