# FDA Inspection 1274624 - Eurofins Donor & Product Testing Inc. - June 27, 2025

Source: https://www.keypedia.com/records/fda_inspections/eurofins-donor-product-testing-inc/1e5ca5ef-98da-4edb-bd45-c3fa6830c256
Source feed: FDA_Inspections

> FDA Inspection 1274624 for Eurofins Donor & Product Testing Inc. on June 27, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1274624
- Company Name: Eurofins Donor & Product Testing Inc.
- Inspection Date: 2025-06-27
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 1274624 - 2025-06-27](https://www.keypedia.com/records/fda_inspections/eurofins-donor-product-testing-inc/8681f2bd-371e-42c9-a058-3f2696b76721)
- [FDA Inspection 1153335 - 2021-09-22](https://www.keypedia.com/records/fda_inspections/eurofins-donor-product-testing-inc/cf5cd871-7d60-40e6-b432-5b272d06e463)

Company: https://www.keypedia.com/companies/eurofins-donor-product-testing-inc/60649756-99e2-4678-9815-133311d789f7

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d