FDA inspection
Medtronic Vascular, Inc.: FDA inspection ending Apr 28, 2000
FDA inspection 22441 · Official Action Indicated (OAI) · Santa Rosa, CA
Key facts
| Inspection ID | 22441 |
|---|---|
| Firm | Medtronic Vascular, Inc. |
| FEI number | 3001452571 |
| Address | 3576 Unocal Pl |
| City | Santa Rosa |
| State | CA |
| ZIP | 95403-1774 |
| Fiscal year | 2000 |
| Inspection end date | Apr 28, 2000 |
| Classification | Official Action Indicated (OAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 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