FDA inspection
Medtronic Perfusion Systems: FDA inspection ending Sep 30, 2016
FDA inspection 987452 · Voluntary Action Indicated (VAI) · Brooklyn Park, MN
Key facts
| Inspection ID | 987452 |
|---|---|
| Firm | Medtronic Perfusion Systems |
| FEI number | 1000116158 |
| Address | 7611 Northland Dr N |
| City | Brooklyn Park |
| State | MN |
| ZIP | 55428 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Sep 30, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| 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