FDA inspection
Medtronic Inc: FDA inspection ending Jul 12, 2006
FDA inspection 433030 · Voluntary Action Indicated (VAI) · Minneapolis, MN
Key facts
| Inspection ID | 433030 |
|---|---|
| Firm | Medtronic Inc |
| FEI number | 3001504994 |
| Address | 710 Medtronic Pkwy Mailstop Ls245 |
| City | Minneapolis |
| State | MN |
| ZIP | 55432-5603 |
| Fiscal year | 2006 |
| Inspection end date | Jul 12, 2006 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None 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