FDA inspection
Revision Optics Inc: FDA inspection ending Aug 9, 2017
FDA inspection 1022506 · No Action Indicated (NAI) · Lake Forest, CA
Key facts
| Inspection ID | 1022506 |
|---|---|
| Firm | Revision Optics Inc |
| FEI number | 3005956347 |
| Address | 25651 Atlantic Ocean Dr Ste A1 |
| City | Lake Forest |
| State | CA |
| ZIP | 92630 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Aug 9, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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