FDA inspection
Iridex Corporation: FDA inspection ending Mar 10, 2003
FDA inspection 261029 · Voluntary Action Indicated (VAI) · Mountain View, CA
Key facts
| Inspection ID | 261029 |
|---|---|
| Firm | Iridex Corporation |
| FEI number | 2939653 |
| Address | 1212 Terra Bella Ave |
| City | Mountain View |
| State | CA |
| ZIP | 94043-1824 |
| Fiscal year | 2003 |
| Inspection end date | Mar 10, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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
- 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