FDA inspection
Evofem Biosciences Inc.: FDA inspection ending Nov 28, 2012
FDA inspection 808507 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 808507 |
|---|---|
| Firm | Evofem Biosciences Inc. |
| FEI number | 1000126925 |
| Address | 12400 High Bluff Dr Ste 600 |
| City | San Diego |
| State | CA |
| ZIP | 92130 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Nov 28, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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
- 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