FDA Inspection 1012443 — EuroAPI UK Limited

EuroAPI UK Limited — FEI 3002807062

The FDA completed an inspection of EuroAPI UK Limited on March 6, 2017 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
March 6, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Haverhill (United Kingdom)