# Unichem Laboratories Ltd., Ghaziabad, India – FDA Inspections

Source: https://www.keypedia.com/companies/unichem-laboratories-ltd/f6920640-950f-4f51-942f-92a6e5fc0e4b

> Inspection records and compliance data for Unichem Laboratories Ltd. in Ghaziabad. 7 FDA inspections on record, 2 Form 483s, last inspected February 13, 2024.

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## Details

- Name: Unichem Laboratories Ltd.
- FEI Number: 3004082076
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK
- Address Line 1: C - 31 & 32 Meerut Road
- City: Ghaziabad
- Country Name: India
- Address: C - 31 & 32 Meerut Road, Ghaziabad, India
- Country: India

## Related Documents

- FDA Inspection 1230023 - Unichem Laboratories Ltd. - 2024-02-13 — classification: No Action Indicated (NAI), source: FDA, date: February 13, 2024
- [FDA Inspection 1102985 - Unichem Laboratories Ltd. - 2019-08-23](https://www.keypedia.com/records/fda_inspections/unichem-laboratories-ltd/36959a18-e9df-4243-b454-13e7ffdc525e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 23, 2019
- FDA Inspection 1087477 - Unichem Laboratories Ltd. - 2019-03-08 — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2019
- FDA Inspection 1053321 - Unichem Laboratories Ltd. - 2018-04-20 — classification: No Action Indicated (NAI), source: FDA, date: April 20, 2018
- [FDA Inspection 1008000 - Unichem Laboratories Ltd. - 2017-03-03](https://www.keypedia.com/records/fda_inspections/unichem-laboratories-ltd/020d0680-36cf-4306-95cd-467bb82ec0a8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 3, 2017
- [FDA Inspection 922881 - Unichem Laboratories Ltd. - 2015-03-27](https://www.keypedia.com/records/fda_inspections/unichem-laboratories-ltd/61e0c092-51ff-434c-9f94-1a5983351232) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2015
- [FDA Inspection 789195 - Unichem Laboratories Ltd. - 2012-06-15](https://www.keypedia.com/records/fda_inspections/unichem-laboratories-ltd/19c406a1-7b2a-4fa6-b263-29575adb753a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 15, 2012

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