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FDA Inspection
•Eurofins Biopharma Product Testing India Private Ltd.•June 20, 2025

Eurofins Biopharma Product Testing India Private Ltd. – FDA Inspection, Jun 20, 2025

Record Details

This FDA Inspection record concerns Eurofins Biopharma Product Testing India Private Ltd., with an inspection on June 20, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Eurofins Biopharma Product Testing India Private Ltd.
Inspection Date
June 20, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Jose M. Cayuela (FDA Associated Person)
View Company Profile

ID · 3924de26-38c7-431d-9a64-bfda466edf6b

Inspection Facts

Inspection number
1277271
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Eurofins Biopharma Product Testing India Private Ltd.

1
DateClassificationOfficeProject area
February 27, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Eurofins Biopharma Product Testing India Private Ltd.
  • FDA Inspection 1085309 - 2019-02-27

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