# Inotiv Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/inotiv-inc/be017b67-b3f0-402d-8a03-b124ca114fa6

> Inspection records and compliance data for Inotiv Inc in West Lafayette, Indiana. Access full analysis and detailed observations.

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## Details

- Name: Inotiv Inc
- FEI Number: 1000140135
- City: West Lafayette
- State: Indiana
- Country Name: United States
- Address Line 1: 2701 Kent Ave
- Zip Code: 47906
- Business Operations: API/FDF ANALYTICAL TESTING, CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING

## Related Documents

- [483 - Inotiv Inc - Unknown Date](https://www.globalkeysolutions.net/records/483/inotiv-inc/1b736eff-c385-4b5e-b117-46a205c800ef) — source: FDA, date: Invalid Date
- [483 - Inotiv Inc - 2025-10-24](https://www.globalkeysolutions.net/records/483/inotiv-inc/541cbd44-f2fe-4fff-adfc-a166d6174e53) — source: FDA, date: October 24, 2025
- [FDA Inspection 1289496 - Inotiv Inc - 2025-10-24](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/3b1a3f6d-9278-4a94-8e5d-6cc5f1b9288d) — source: FDA, date: October 24, 2025
- [FDA Inspection 1289496 - Inotiv Inc - 2025-10-24](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/5febaac7-35c0-43c9-bebf-7f009167ed89) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 24, 2025
- [FDA Inspection 1100971 - Inotiv Inc - 2019-07-26](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/1fe116df-2ba0-42cb-ae88-e03f7c2ad809) — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2019
- [FDA Inspection 1078296 - Inotiv Inc - 2018-12-07](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/0735b29c-9935-4f1f-a0d0-88c57f417d1f) — classification: No Action Indicated (NAI), source: FDA, date: December 7, 2018
- [FDA Inspection 1038421 - Inotiv Inc - 2018-01-11](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/5b84c81e-8204-40f7-9f81-ae1956c97285) — classification: No Action Indicated (NAI), source: FDA, date: January 11, 2018
- [FDA Inspection 848016 - Inotiv Inc - 2013-09-12](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/aaa042d4-c002-45db-b227-362b28ff2bb7) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2013
- [FDA Inspection 821844 - Inotiv Inc - 2013-03-08](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/8e814265-873e-4a36-9a20-9c6670f9e816) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 8, 2013
- [FDA Inspection 773057 - Inotiv Inc - 2012-03-19](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/803b7414-52e0-4f38-96ea-b8a96b8c16d6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 19, 2012
- [FDA Inspection 710326 - Inotiv Inc - 2011-01-24](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/be2943a4-db6e-4f6d-b643-73dd6591329a) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2011
- [FDA Inspection 710326 - Inotiv Inc - 2011-01-24](https://www.globalkeysolutions.net/records/fda_inspections/inotiv-inc/da076b90-b434-4387-8e52-0c2c7019c3bf) — classification: No Action Indicated (NAI), source: FDA, date: January 24, 2011

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