# Lupin Limited, Mandideep, India – FDA Inspections

Source: https://www.keypedia.com/companies/lupin-limited/122cdc90-be58-47a6-8127-004b3a6a04c3

> Inspection records and compliance data for Lupin Limited in Mandideep. 6 FDA inspections on record (3 OAI), 1 Form 483, last inspected November 23, 2022.

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## Details

- Name: Lupin Limited
- FEI Number: 3002807511
- Facility Type: Pharmaceutical Manufacturer
- Business Operations: API MANUFACTURE, FDF MANUFACTURE, PACK
- Address Line 1: Unit 1, 198 - 202 New Ind Area No 2
- City: Mandideep
- Country Name: India
- Address: Unit 1, 198 - 202 New Ind Area No 2, Mandideep, India
- Country: India

## Related Documents

- [483 - Lupin Limited - 2022-11-23](https://www.keypedia.com/records/483/lupin-limited/9526924e-9742-43cf-b424-a50ea10b302e) — source: FDA, date: November 23, 2022
- [FDA Inspection 1191374 - Lupin Limited - 2022-11-23](https://www.keypedia.com/records/fda_inspections/lupin-limited/f9abe983-6d55-453b-b290-d2772c179cf1) — classification: Official Action Indicated (OAI), source: FDA, date: November 23, 2022
- [483 - Lupin Limited - 2018-12-04](https://www.keypedia.com/records/483/lupin-limited/7563e21c-3de3-472c-b7c2-896029346d00) — source: FDA, date: December 4, 2018
- [FDA Inspection 1073522 - Lupin Limited - 2018-12-04](https://www.keypedia.com/records/fda_inspections/lupin-limited/03c79b3f-853f-4b7e-9073-4ea004189e1c) — classification: Official Action Indicated (OAI), source: FDA, date: December 4, 2018
- FDA Inspection 962120 - Lupin Limited - 2016-02-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 19, 2016
- FDA Inspection 748307 - Lupin Limited - 2011-09-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 23, 2011
- FDA Inspection 632615 - Lupin Limited - 2009-11-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 30, 2009
- [FDA Inspection 552469 - Lupin Limited - 2008-11-12](https://www.keypedia.com/records/fda_inspections/lupin-limited/f03e1a61-858c-4c3c-84f8-056f5e74ee7f) — classification: Official Action Indicated (OAI), source: FDA, date: November 12, 2008

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