FDA inspection
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF): FDA inspection ending Oct 19, 1999
FDA inspection 1013 · No Action Indicated (NAI) · Mounds View, MN
Key facts
| Inspection ID | 1013 |
|---|---|
| Firm | Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) |
| FEI number | 2182208 |
| Address | 8200 Coral Sea St Ne |
| City | Mounds View |
| State | MN |
| ZIP | 55112-4391 |
| Fiscal year | 2000 |
| Inspection end date | Oct 19, 1999 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| 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
- 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