FDA inspection
Inotiv Inc: FDA inspection ending Dec 7, 2018
FDA inspection 1078296 · No Action Indicated (NAI) · West Lafayette, IN
Key facts
| Inspection ID | 1078296 |
|---|---|
| Firm | Inotiv Inc |
| FEI number | 1000140135 |
| Address | 2701 Kent Ave |
| City | West Lafayette |
| State | IN |
| ZIP | 47906 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Dec 7, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Bioresearch Monitoring |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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