# V-Ensure Pharma Technologies Pvt. Limited, Raigad, India – FDA Inspections

Source: https://www.keypedia.com/companies/v-ensure-pharma-technologies-pvt-limited/01233430-1062-49f9-ad93-adf95ab293e8

> Inspection records and compliance data for V-Ensure Pharma Technologies Pvt. Limited in Raigad. 3 FDA inspections on record, 1 Form 483, last inspected May 17, 2024.

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## Details

- Name: V-Ensure Pharma Technologies Pvt. Limited
- FEI Number: 3012155344
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK
- Address Line 1: N - 32 Additional Patalganga Midc, Village Badruk Karade
- City: Raigad
- Country Name: India
- Address: N - 32 Additional Patalganga Midc, Village Badruk Karade, Raigad, India
- Country: India

## Related Documents

- [483 - V-Ensure Pharma Technologies Pvt. Limited - 2024-05-17](https://www.keypedia.com/records/483/v-ensure-pharma-technologies-pvt-limited/d38bf8f3-655a-4884-bbbc-05a2a84640ce) — source: FDA, date: May 17, 2024
- [FDA Inspection 1238720 - V-Ensure Pharma Technologies Pvt. Limited - 2024-05-17](https://www.keypedia.com/records/fda_inspections/v-ensure-pharma-technologies-pvt-limited/df0b53a9-89f6-4620-9efa-7120e3ccf3b5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 17, 2024
- FDA Inspection 1238720 - V-Ensure Pharma Technologies Pvt. Limited - 2024-05-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 17, 2024
- [483 - V-Ensure Pharma Technologies Pvt. Limited - 2023-01-27](https://www.keypedia.com/records/483/v-ensure-pharma-technologies-pvt-limited/f40e8805-b189-49dc-a34c-d7be69837328) — source: FDA, date: January 27, 2023
- [FDA Inspection 1196630 - V-Ensure Pharma Technologies Pvt. Limited - 2023-01-27](https://www.keypedia.com/records/fda_inspections/v-ensure-pharma-technologies-pvt-limited/3b692e59-7b0a-4147-9e11-4f6dbfa87123) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2023
- FDA Inspection 1122917 - V-Ensure Pharma Technologies Pvt. Limited - 2020-02-26 — classification: No Action Indicated (NAI), source: FDA, date: February 26, 2020

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