FDA Inspection 965116 — Ipsen BioPharm Ltd

Ipsen BioPharm Ltd — FEI 1000346340

The FDA completed an inspection of Ipsen BioPharm Ltd on January 20, 2016 in Wrexham. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 20, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wrexham (United Kingdom)