# Eurofins Donor & Product Testing Inc Minneapolis – FDA Inspection, Jan 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 of Eurofins Donor & Product Testing Inc Minneapolis, January 22, 2025. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Center: Biologics
- Office Name: Center for Biologics Evaluation and Research
- Citation Count: 0

## Related Documents

- FDA Inspection 1077570 - 2018-12-14

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/kellie-l-thommes/255a1b92-cd56-41f5-9622-82e8a629e153)

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