FDA inspection
Medtronic Perfusion Systems: FDA inspection ending Nov 19, 2012
FDA inspection 808091 · No Action Indicated (NAI) · Parker, CO
Key facts
| Inspection ID | 808091 |
|---|---|
| Firm | Medtronic Perfusion Systems |
| FEI number | 1718389 |
| Address | 18501 Plaza Dr |
| City | Parker |
| State | CO |
| ZIP | 80134 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Nov 19, 2012 |
| 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
- 1–9 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