FDA inspection
Earlens Corporation: FDA inspection ending Oct 30, 2019
FDA inspection 1121817 · Voluntary Action Indicated (VAI) · Menlo Park, CA
Key facts
| Inspection ID | 1121817 |
|---|---|
| Firm | Earlens Corporation |
| FEI number | 3010863048 |
| Address | 4045A Campbell Ave |
| City | Menlo Park |
| State | CA |
| ZIP | 94025-1006 |
| Fiscal year | 2020 |
| Inspection end date | Oct 30, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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
- 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