# Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.) - Inspection Records

Source: https://www.keypedia.com/companies/amoli-organics-a-division-of-umedica-laboratories-pvt-ltd/b8bc3797-9fd3-4e78-a475-bc53b2f5310e

> Inspection records and compliance data for Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.) in Padra, None. Access full analysis and detailed observations.

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## Details

- Name: Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.)
- FEI Number: 3007836955
- City: Padra
- State: None
- Country Name: India
- Address Line 1: Block No, 422 Village: Luna; E C P Canal Road
- Zip Code: None
- Business Operations: API MANUFACTURE

## Related Documents

- [483 - Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.) - 2024-01-12](https://www.keypedia.com/records/483/amoli-organics-a-division-of-umedica-laboratories-pvt-ltd/e42a8772-2a37-49c9-8ae2-b055a0afce96) — source: FDA, date: January 12, 2024
- [483 - Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.) - 2024-01-12](https://www.keypedia.com/records/483/amoli-organics-a-division-of-umedica-laboratories-pvt-ltd/471bdde7-299f-4ea1-9252-d11732985613) — source: FDA, date: January 12, 2024
- [FDA Inspection 1227272 - Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.) - 2024-01-12](https://www.keypedia.com/records/fda_inspections/amoli-organics-a-division-of-umedica-laboratories-pvt-ltd/5273dd21-7c11-4e0f-863e-29a17582ef00) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 12, 2024
- [483 - Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.) - 2024-01-08](https://www.keypedia.com/records/483/amoli-organics-a-division-of-umedica-laboratories-pvt-ltd/a38281dd-dc32-49b6-bbc5-a5ed0ed10ea2) — source: FDA, date: January 8, 2024
- [FDA Inspection 986258 - Amoli Organics (A Division of Umedica Laboratories Pvt. Ltd.) - 2016-08-20](https://www.keypedia.com/records/fda_inspections/amoli-organics-a-division-of-umedica-laboratories-pvt-ltd/b265cef3-87e8-4bb9-af63-455e766fc878) — classification: No Action Indicated (NAI), source: FDA, date: August 20, 2016

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