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FDA Inspection
•Eurofins BioPharma Product Testing Spain SLU•November 6, 2018

Eurofins BioPharma Product Testing Spain SLU – FDA Inspection, Nov 6, 2018

Record Details

This FDA Inspection record concerns Eurofins BioPharma Product Testing Spain SLU, with an inspection on November 6, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Eurofins BioPharma Product Testing Spain SLU
Inspection Date
November 6, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • MRA MunizN (Issuing Officer)
View Company Profile

ID · 2449d1dd-d952-445b-9749-0e72188f38a5

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1134791
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Eurofins BioPharma Product Testing Spain SLU

3
DateClassificationOfficeProject area
June 19, 2025Not classifiedOffice of Inspections and Investigations
January 13, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 29, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Eurofins BioPharma Product Testing Spain SLU
  • FDA Inspection 1279238 - 2025-06-19
  • FDA Inspection 1285158 - 2022-01-13
  • FDA Inspection 986616 - 2016-06-29

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