# FDA Inspection 1277271 - Eurofins Biopharma Product Testing India Private Ltd. - June 20, 2025

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-india-private-ltd/6f42a3fc-d78a-4e85-94ab-e1af65c40da3
Source feed: FDA_Inspections

> FDA Inspection 1277271 for Eurofins Biopharma Product Testing India Private Ltd. on June 20, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1277271
- Company Name: Eurofins Biopharma Product Testing India Private Ltd.
- Inspection Date: 2025-06-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 1277271 - 2025-06-20](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-india-private-ltd/3924de26-38c7-431d-9a64-bfda466edf6b)
- [FDA Inspection 1085309 - 2019-02-27](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-india-private-ltd/1bd35c45-36a5-4023-9435-d1b8e4eae8e3)

Company: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-india-private-ltd/3bf38a57-43cd-47f1-bade-72b277baf1e7

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c