FDA inspection
Iridex Corporation: FDA inspection ending Sep 20, 2023
FDA inspection 1218928 · Voluntary Action Indicated (VAI) · Mountain View, CA
Key facts
| Inspection ID | 1218928 |
|---|---|
| Firm | Iridex Corporation |
| FEI number | 2939653 |
| Address | 1212 Terra Bella Ave |
| City | Mountain View |
| State | CA |
| ZIP | 94043 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | Sep 20, 2023 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Radiation Control and Health Safety Act |
| 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
- 10–99 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