FDA inspection
Medtronic Neuromodulation: FDA inspection ending May 9, 2012
FDA inspection 774200 · Official Action Indicated (OAI) · Minneapolis, MN
Key facts
| Inspection ID | 774200 |
|---|---|
| Firm | Medtronic Neuromodulation |
| FEI number | 2182207 |
| Address | 7000 Central Ave Ne |
| City | Minneapolis |
| State | MN |
| ZIP | 55432 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | May 9, 2012 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 324638 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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