# Srini Pharmaceuticals Private Limited - Inspection Records

Source: https://www.keypedia.com/companies/srini-pharmaceuticals-private-limited/a94a3542-6c22-4004-b897-6bd2c9019c14

> Inspection records and compliance data for Srini Pharmaceuticals Private Limited in Chotuppal, None. Access full analysis and detailed observations.

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## Details

- Name: Srini Pharmaceuticals Private Limited
- FEI Number: 3004015257
- City: Chotuppal
- State: None
- Country Name: India
- Address Line 1: S. No. 247 Chotuppal Mandal Village, Nalgonda District
- Zip Code: None
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1110654 - Srini Pharmaceuticals Private Limited - 2019-10-18](https://www.keypedia.com/records/fda_inspections/srini-pharmaceuticals-private-limited/9dd1e874-78cd-4753-88ba-772af5496bc5) — classification: No Action Indicated (NAI), source: FDA, date: October 18, 2019
- [FDA Inspection 1041495 - Srini Pharmaceuticals Private Limited - 2017-10-27](https://www.keypedia.com/records/fda_inspections/srini-pharmaceuticals-private-limited/9bd24d04-9fe0-43f2-9805-3b444b184e09) — classification: No Action Indicated (NAI), source: FDA, date: October 27, 2017
- [FDA Inspection 923934 - Srini Pharmaceuticals Private Limited - 2015-04-24](https://www.keypedia.com/records/fda_inspections/srini-pharmaceuticals-private-limited/e4143d20-7afe-4e47-a1aa-165809c9609d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2015
- [FDA Inspection 793843 - Srini Pharmaceuticals Private Limited - 2012-07-19](https://www.keypedia.com/records/fda_inspections/srini-pharmaceuticals-private-limited/1672ba18-103b-4607-836b-2928e320db45) — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2012
- [FDA Inspection 577785 - Srini Pharmaceuticals Private Limited - 2009-04-02](https://www.keypedia.com/records/fda_inspections/srini-pharmaceuticals-private-limited/c0d93316-8985-4a89-8106-54c635e07adc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 2, 2009

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