FDA inspection
Inovise Medical, Inc.: FDA inspection ending Mar 21, 2013
FDA inspection 823440 · Voluntary Action Indicated (VAI) · Beaverton, OR
Key facts
| Inspection ID | 823440 |
|---|---|
| Firm | Inovise Medical, Inc. |
| FEI number | 3003264460 |
| Address | 8770 SW Nimbus Ave Ste D |
| City | Beaverton |
| State | OR |
| ZIP | 97008 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Mar 21, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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