FDA inspection
Stryker Neurovascular, Inc.: FDA inspection ending Feb 2, 2009
FDA inspection 561509 · No Action Indicated (NAI) · Salt Lake City, UT
Key facts
| Inspection ID | 561509 |
|---|---|
| Firm | Stryker Neurovascular, Inc. |
| FEI number | 3012931345 |
| Address | 4870 West 2100 South |
| City | Salt Lake City |
| State | UT |
| ZIP | 84120 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Feb 2, 2009 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: 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