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FDA Inspection
•Eurofins Donor & Product Testing, Inc. Philadelphia•December 12, 2025

Eurofins Donor & Product Testing, Inc. Philadelphia – FDA Inspection, Dec 12, 2025

Record Details

This FDA Inspection record concerns Eurofins Donor & Product Testing, Inc. Philadelphia, with an inspection on December 12, 2025, issued by the Philadelphia District Office, covering biologics.

Company
Eurofins Donor & Product Testing, Inc. Philadelphia
Inspection Date
December 12, 2025
Product Type
Biologics
Office
Philadelphia District Office
Person
  • Emily A. Walters (Company Rep)
View Company Profile

ID · e8ec8d89-151e-46b5-a6c5-754f7f6b975a

Inspection Facts

Inspection number
1296050
FDA center
Biologics

Other FDA inspections of Eurofins Donor & Product Testing, Inc. Philadelphia

6
DateClassificationOfficeProject area
February 17, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 28, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 9, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 21, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 14, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Eurofins Donor & Product Testing, Inc. Philadelphia
  • FDA Inspection 1198943 - 2023-02-17
  • FDA Inspection 1106739 - 2019-08-28
  • FDA Inspection 974569 - 2016-06-09
  • FDA Inspection 875463 - 2014-04-21
  • FDA Inspection 800068 - 2012-09-14

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