FDA inspection
Medtronic Navigation, Inc.: FDA inspection ending Sep 30, 2019
FDA inspection 1103549 · Voluntary Action Indicated (VAI) · Lafayette, CO
Key facts
| Inspection ID | 1103549 |
|---|---|
| Firm | Medtronic Navigation, Inc. |
| FEI number | 1000517638 |
| Address | 826 Coal Creek Cir |
| City | Lafayette |
| State | CO |
| ZIP | 80026 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Sep 30, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 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