FDA inspection
Vitrolife Inc.: FDA inspection ending Aug 19, 2021
FDA inspection 1149812 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 1149812 |
|---|---|
| Firm | Vitrolife Inc. |
| FEI number | 3002757762 |
| Address | 6835 Flanders Dr Ste 500 |
| City | San Diego |
| State | CA |
| ZIP | 92121 |
| Country | United States |
| Fiscal year | 2021 |
| Inspection end date | Aug 19, 2021 |
| 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