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FDA Inspection
•Eurofins BioPharma Product Testing Columbia, LLC•January 14, 2022

Eurofins BioPharma Product Testing Columbia, LLC – FDA Inspection, Jan 14, 2022

Record Details

This FDA Inspection record concerns Eurofins BioPharma Product Testing Columbia, LLC, with an inspection on January 14, 2022, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Eurofins BioPharma Product Testing Columbia, LLC
Inspection Date
January 14, 2022
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · eba63794-537e-48f1-a247-1601e534152e

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1161343
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Eurofins BioPharma Product Testing Columbia, LLC

7
DateClassificationOfficeProject area
December 4, 2024Not classifiedKansas City District Office
August 15, 2018Not classifiedKansas City District Office
January 26, 2017Not classifiedKansas City District Office
March 6, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 18, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Eurofins BioPharma Product Testing Columbia, LLC
  • FDA Inspection 1258161 - 2024-12-04
  • FDA Inspection 1065874 - 2018-08-15
  • FDA Inspection 999122 - 2017-01-26
  • FDA Inspection 917473 - 2015-03-06
  • FDA Inspection 791170 - 2012-07-18

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