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FDA Inspection
•Eurofins Donor & Product Testing, Inc. Philadelphia•August 28, 2019

Eurofins Donor & Product Testing, Inc. Philadelphia – FDA Inspection, Aug 28, 2019

Record Details

This FDA Inspection record concerns Eurofins Donor & Product Testing, Inc. Philadelphia, with an inspection on August 28, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Eurofins Donor & Product Testing, Inc. Philadelphia
Inspection Date
August 28, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Kish Bolden (Issuing Officer)
View Company Profile

ID · be37e084-a4ac-47e9-b62e-a9078f535ee6

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1106739
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

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

6
DateClassificationOfficeProject area
December 12, 2025Not classifiedPhiladelphia District Office
February 17, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
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 1296050 - 2025-12-12
  • FDA Inspection 1198943 - 2023-02-17
  • FDA Inspection 974569 - 2016-06-09
  • FDA Inspection 875463 - 2014-04-21
  • FDA Inspection 800068 - 2012-09-14

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