FDA inspection
Medtronic Sofamor Danek USA, Inc: FDA inspection ending Feb 27, 2008
FDA inspection 509963 · No Action Indicated (NAI) · Memphis, TN
Key facts
| Inspection ID | 509963 |
|---|---|
| Firm | Medtronic Sofamor Danek USA, Inc |
| FEI number | 3003120897 |
| Address | 4340 Swinnea Rd |
| City | Memphis |
| State | TN |
| ZIP | 38118-6603 |
| Fiscal year | 2008 |
| Inspection end date | Feb 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
- 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