FDA Inspection 1155931 — EuroAPI UK Limited

EuroAPI UK Limited — FEI 3002807062

The FDA completed an inspection of EuroAPI UK Limited on July 22, 2019 in Haverhill. 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
July 22, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Haverhill (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)