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FDA Inspection
•Eurofins BioPharma Product Testing Hamburg GmbH•July 10, 2013

Eurofins BioPharma Product Testing Hamburg GmbH – FDA Inspection, Jul 10, 2013

Record Details

This FDA Inspection record concerns Eurofins BioPharma Product Testing Hamburg GmbH, with an inspection on July 10, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Eurofins BioPharma Product Testing Hamburg GmbH
Inspection Date
July 10, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 32d370fa-6547-4426-ba48-4931d6e2e9c9

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
841999
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Eurofins BioPharma Product Testing Hamburg GmbH

2
DateClassificationOfficeProject area
October 19, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 18, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Eurofins BioPharma Product Testing Hamburg GmbH
  • FDA Inspection 1288412 - 2022-10-19
  • FDA Inspection 1109935 - 2019-09-18

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