FDA Inspection 1134791 — Eurofins BioPharma Product Testing Spain SLU

Eurofins BioPharma Product Testing Spain SLU — FEI 3007914833

The FDA completed an inspection of Eurofins BioPharma Product Testing Spain SLU on November 6, 2018 in Esplugues De Llobregat. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 6, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Esplugues De Llobregat (Spain)

Additional Details

Mutual Recognition Agreement (MRA)