FDA inspection
Medtronic Perfusion Systems: FDA inspection ending Jun 24, 2014
FDA inspection 886720 · No Action Indicated (NAI) · Brooklyn Park, MN
Key facts
| Inspection ID | 886720 |
|---|---|
| Firm | Medtronic Perfusion Systems |
| FEI number | 1000116158 |
| Address | 7611 Northland Dr N |
| City | Brooklyn Park |
| State | MN |
| ZIP | 55428 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Jun 24, 2014 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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