FDA inspection
Medtronic Inc: FDA inspection ending Jun 23, 2009
FDA inspection 598225 · No Action Indicated (NAI) · Omaha, NE
Key facts
| Inspection ID | 598225 |
|---|---|
| Firm | Medtronic Inc |
| FEI number | 3003418152 |
| Address | 440 Regency Parkway Dr Ste 130 |
| City | Omaha |
| State | NE |
| ZIP | 68114 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jun 23, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
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