FDA inspection
Cerovene Inc.: FDA inspection ending Mar 23, 2026
FDA inspection 1308838 · Voluntary Action Indicated (VAI) · Valley Cottage, NY
Key facts
| Inspection ID | 1308838 |
|---|---|
| Firm | Cerovene Inc. |
| FEI number | 3005890568 |
| Address | 612 Corporate Way Ste 10 |
| City | Valley Cottage |
| State | NY |
| ZIP | 10989 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Mar 23, 2026 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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