FDA inspection
Bentley Laboratories LLC: FDA inspection ending Mar 27, 2026
FDA inspection 1280817 · Official Action Indicated (OAI) · Edison, NJ
Key facts
| Inspection ID | 1280817 |
|---|---|
| Firm | Bentley Laboratories LLC |
| FEI number | 2244819 |
| Address | 111 Fieldcrest Ave |
| City | Edison |
| State | NJ |
| ZIP | 08837 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | Mar 27, 2026 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
| Warning letter | 732028 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes 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