FDA inspection
Medtronic Vascular, Inc.: FDA inspection ending Jun 19, 2009
FDA inspection 595178 · No Action Indicated (NAI) · Santa Rosa, CA
Key facts
| Inspection ID | 595178 |
|---|---|
| Firm | Medtronic Vascular, Inc. |
| FEI number | 3005364322 |
| Address | 3850 Brickway Blvd |
| City | Santa Rosa |
| State | CA |
| ZIP | 95403 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jun 19, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Postmarket Assurance: 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