FDA inspection
Medtronic Perfusion Systems: FDA inspection ending Jan 28, 2005
FDA inspection 369219 · Parker, CO
Key facts
| Inspection ID | 369219 |
|---|---|
| Firm | Medtronic Perfusion Systems |
| FEI number | 1718389 |
| Address | 18501 Plaza Dr |
| City | Parker |
| State | CO |
| ZIP | 80134-9061 |
| Fiscal year | 2005 |
| Inspection end date | Jan 28, 2005 |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes 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