# FDA Inspection 1280309 - Eurofins Biopharma Product Testing Ireland Limited - June 20, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/85fbc605-0972-4295-919d-4e91789b7fbb
Source feed: FDA_Inspections

> FDA Inspection 1280309 for Eurofins Biopharma Product Testing Ireland Limited on June 20, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280309
- Company Name: Eurofins Biopharma Product Testing Ireland Limited
- Inspection Date: 2025-06-20
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics

## Related Documents

- [FDA Inspection 1280309 - 2025-06-20](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/b5a5f352-2caa-41a6-9648-3cf3e17a1fb4)
- [FDA Inspection 1280309 - 2025-06-20](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/d834f021-236c-4005-a28f-ca4dfc3bd67b)
- [FDA Inspection 1270954 - 2023-05-26](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/de6f5a0e-d3e9-4a64-a2b4-e5f938b251fa)
- [FDA Inspection 1008821 - 2017-02-24](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/8470fa32-888d-4e85-be16-9e50d5047442)
- [FDA Inspection 826551 - 2013-03-29](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/e5bd4b8f-5bb6-4e4e-ad38-35e24505d475)

Company: https://www.globalkeysolutions.net/companies/eurofins-biopharma-product-testing-ireland-limited/2cded381-226c-436d-b95e-6f1b70b922d2