FDA inspection
Medtronic, Inc.: FDA inspection ending May 14, 2018
FDA inspection 1052017 · Official Action Indicated (OAI) · Mounds View, MN
Key facts
| Inspection ID | 1052017 |
|---|---|
| Firm | Medtronic, Inc. |
| FEI number | 2182208 |
| Address | 8200 Coral Sea St Ne |
| City | Mounds View |
| State | MN |
| ZIP | 55112 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | May 14, 2018 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 560736 |
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