FDA inspection
Gynex Corporation: FDA inspection ending Apr 25, 2014
FDA inspection 876242 · Voluntary Action Indicated (VAI) · Redmond, WA
Key facts
| Inspection ID | 876242 |
|---|---|
| Firm | Gynex Corporation |
| FEI number | 3001238683 |
| Address | 14603 NE 87th St |
| City | Redmond |
| State | WA |
| ZIP | 98052 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Apr 25, 2014 |
| 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