# Harman Finochem Limited - Inspection Records

Source: https://www.globalkeysolutions.net/companies/harman-finochem-limited/7622941a-bad2-45c3-bd91-07d2bb63f905

> Inspection records and compliance data for Harman Finochem Limited in Aurangabad, None. Access full analysis and detailed observations.

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## Details

- Name: Harman Finochem Limited
- FEI Number: 3003130103
- City: Aurangabad
- State: None
- Country Name: India
- Address Line 1: Industrial Area Chikalthana, Plot No. E-7, E-8, E-9 & E-53 M.I.D.C.
- Zip Code: None
- Business Operations: API MANUFACTURE

## Related Documents

- [FDA Inspection 1236559 - Harman Finochem Limited - 2024-03-22](https://www.globalkeysolutions.net/records/fda_inspections/harman-finochem-limited/541bf9ee-4a7a-4c45-92a2-1e57b15f4a92) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 22, 2024
- [483 - Harman Finochem Limited - 2024-03-18](https://www.globalkeysolutions.net/records/483/harman-finochem-limited/21b993cf-a4a3-45d8-bb8e-2c7561d4da21) — source: FDA, date: March 18, 2024
- [FDA Inspection 1063013 - Harman Finochem Limited - 2018-07-20](https://www.globalkeysolutions.net/records/fda_inspections/harman-finochem-limited/b7ee643c-ce02-44ff-874c-d9e828aa9a73) — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2018
- [FDA Inspection 919251 - Harman Finochem Limited - 2015-03-27](https://www.globalkeysolutions.net/records/fda_inspections/harman-finochem-limited/8de341bc-4c85-48cb-9ff7-bc31725e64e3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 27, 2015
- [FDA Inspection 802558 - Harman Finochem Limited - 2012-06-12](https://www.globalkeysolutions.net/records/fda_inspections/harman-finochem-limited/81b657b7-3bc9-401f-b3f0-12410d2cd87e) — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2012
- [FDA Inspection 590431 - Harman Finochem Limited - 2009-04-09](https://www.globalkeysolutions.net/records/fda_inspections/harman-finochem-limited/c25a4bed-7299-485f-bdb7-b0938e294407) — classification: No Action Indicated (NAI), source: FDA, date: April 9, 2009

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