FDA inspection
Medtronic Heart Valve Division: FDA inspection ending Dec 8, 2005
FDA inspection 405050 · Voluntary Action Indicated (VAI) · Spring Lake Park, MN
Key facts
| Inspection ID | 405050 |
|---|---|
| Firm | Medtronic Heart Valve Division |
| FEI number | 2127690 |
| Address | 8299 Central Ave Ne |
| City | Spring Lake Park |
| State | MN |
| ZIP | 55432-2023 |
| Fiscal year | 2006 |
| Inspection end date | Dec 8, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med 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
- 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