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FDA Inspection
•Eurofins Donor & Product Testing Inc Minneapolis•January 22, 2025

Eurofins Donor & Product Testing Inc Minneapolis – FDA Inspection, Jan 22, 2025

Record Details

This FDA Inspection record concerns Eurofins Donor & Product Testing Inc Minneapolis, with an inspection on January 22, 2025, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Eurofins Donor & Product Testing Inc Minneapolis
Inspection Date
January 22, 2025
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Kellie L. Thommes (FDA Associated Person)
View Company Profile

ID · bf47286b-b30e-4749-ada5-1547af1df4ca

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1259801
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Eurofins Donor & Product Testing Inc Minneapolis

1
DateClassificationOfficeProject area
December 14, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Eurofins Donor & Product Testing Inc Minneapolis
  • FDA Inspection 1077570 - 2018-12-14

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