# FDA Inspection 1259801 - Eurofins Donor & Product Testing Inc Minneapolis - January 22, 2025

Source: https://www.keypedia.com/records/fda_inspections/eurofins-donor-product-testing-inc-minneapolis/bf47286b-b30e-4749-ada5-1547af1df4ca
Source feed: FDA_Inspections

> FDA Inspection 1259801 for Eurofins Donor & Product Testing Inc Minneapolis on January 22, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1259801
- Company Name: Eurofins Donor & Product Testing Inc Minneapolis
- Inspection Date: 2025-01-22
- 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 1259801 - 2025-01-22](https://www.keypedia.com/records/fda_inspections/eurofins-donor-product-testing-inc-minneapolis/63caec26-d3ac-4ee1-b722-223898322236)
- [FDA Inspection 1077570 - 2018-12-14](https://www.keypedia.com/records/fda_inspections/eurofins-donor-product-testing-inc-minneapolis/cd7900f9-af25-4f12-a6bc-ce29c0c5bd9f)

Company: https://www.keypedia.com/companies/eurofins-donor-product-testing-inc-minneapolis/fd6f9676-1658-4c98-9515-6e99c0d51837

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