FDA Inspection 1289496 — Inotiv Inc

Inotiv Inc — FEI 1000140135

The FDA completed an inspection of Inotiv Inc on October 24, 2025 in West Lafayette, IN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 24, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
West Lafayette, IN (United States)

Additional Details

Bioanalytical BA/BE