FDA inspection
Vioptix, Inc.: FDA inspection ending Aug 21, 2023
FDA inspection 1218185 · No Action Indicated (NAI) · Newark, CA
Key facts
| Inspection ID | 1218185 |
|---|---|
| Firm | Vioptix, Inc. |
| FEI number | 3003965364 |
| Address | 39655 Eureka Dr |
| City | Newark |
| State | CA |
| ZIP | 94560-4806 |
| Fiscal year | 2023 |
| Inspection end date | Aug 21, 2023 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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