# Torrent Pharmaceuticals Limited, Gandhi Nagar, India – FDA Inspections

Source: https://www.keypedia.com/companies/torrent-pharmaceuticals-limited/3132b954-14e5-4ee9-bf30-7ae06ff6899e

> Inspection records and compliance data for Torrent Pharmaceuticals Limited in Gandhi Nagar. 5 FDA inspections on record, 1 Form 483, 1 warning letter, last inspected October 04, 2024.

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## Details

- Name: Torrent Pharmaceuticals Limited
- FEI Number: 3007078804
- Business Operations: CLINICAL BIOEQUIVALENCE OR BIOAVAILABILITY STUDY, IN VITRO BIOEQUIVALENCE OR BIOANALYTICAL TESTING
- Address Line 1: Near Kanoria Hospital
- City: Gandhi Nagar
- Country Name: India
- Address: Near Kanoria Hospital, Gandhi Nagar, India
- Country: India

## Related Documents

- FDA Inspection 1256784 - Torrent Pharmaceuticals Limited - 2024-10-04 — source: FDA, date: October 4, 2024
- FDA Inspection 1256784 - Torrent Pharmaceuticals Limited - 2024-10-04 — classification: No Action Indicated (NAI), source: FDA, date: October 4, 2024
- FDA Inspection 1161232 - Torrent Pharmaceuticals Limited - 2021-12-15 — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2021
- [WARNING_LETTER - Torrent Pharmaceuticals Limited - 2019-04-16](https://www.keypedia.com/records/warning_letter/torrent-pharmaceuticals-limited/583a9d53-65a7-4e88-acde-bed7b7c89bf4) — source: FDA, date: April 16, 2019
- FDA Inspection 1055697 - Torrent Pharmaceuticals Limited - 2018-06-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2018
- [FDA Inspection 1055697 - Torrent Pharmaceuticals Limited - 2018-06-15](https://www.keypedia.com/records/fda_inspections/torrent-pharmaceuticals-limited/fc876dbe-932e-49d4-9b1b-841a0c89aa10) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2018
- FDA Inspection 1051188 - Torrent Pharmaceuticals Limited - 2018-02-28 — classification: No Action Indicated (NAI), source: FDA, date: February 28, 2018
- FDA Inspection 1038709 - Torrent Pharmaceuticals Limited - 2017-12-04 — source: FDA, date: December 4, 2017

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