FDA inspection
Kerber USA Inc.: FDA inspection ending Nov 7, 2025
FDA inspection 1291292 · Voluntary Action Indicated (VAI) · Amherst, NY
Key facts
| Inspection ID | 1291292 |
|---|---|
| Firm | Kerber USA Inc. |
| FEI number | 3017419219 |
| Address | 1576 Sweet Home Rd Ste 102b |
| City | Amherst |
| State | NY |
| ZIP | 14228 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Nov 7, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 10–99 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