# Anjan Drug Private Limited, Alathur, India – FDA Inspections

Source: https://www.keypedia.com/companies/anjan-drug-private-limited/d722af5c-422c-43d5-8f53-6a3d4b8d84de

> Inspection records and compliance data for Anjan Drug Private Limited in Alathur. 6 FDA inspections on record, 2 Form 483s, last inspected July 11, 2025.

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## Details

- Name: Anjan Drug Private Limited
- FEI Number: 3005782924
- Business Operations: API MANUFACTURE
- Address Line 1: Plot Nos 109 110 115 & 116, Sidco Pharmaceutical Industrial Estate, Old Mahabalipuram Road
- City: Alathur
- Country Name: India
- Address: Plot Nos 109 110 115 & 116, Sidco Pharmaceutical Industrial Estate, Old Mahabalipuram Road, Alathur, India
- Country: India

## Related Documents

- [FDA Inspection 1277816 - Anjan Drug Private Limited - 2025-07-11](https://www.keypedia.com/records/fda_inspections/anjan-drug-private-limited/fed41059-18ae-4046-b795-e85aa217a078) — source: FDA, date: July 11, 2025
- FDA Inspection 1277816 - Anjan Drug Private Limited - 2025-07-11 — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2025
- FDA Inspection 1119748 - Anjan Drug Private Limited - 2020-01-31 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 31, 2020
- [FDA Inspection 1101857 - Anjan Drug Private Limited - 2019-08-16](https://www.keypedia.com/records/fda_inspections/anjan-drug-private-limited/c8f9386c-6f7e-48e5-bf56-4ee7128b399f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 16, 2019
- [FDA Inspection 1059806 - Anjan Drug Private Limited - 2018-07-19](https://www.keypedia.com/records/fda_inspections/anjan-drug-private-limited/d0a9e89c-f76b-4ad8-a4d3-18c3ac5121bd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 19, 2018
- FDA Inspection 957358 - Anjan Drug Private Limited - 2016-01-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2016
- FDA Inspection 836031 - Anjan Drug Private Limited - 2013-04-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 11, 2013

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