FDA Inspection 1059005 — Ipsen BioPharm Ltd

Ipsen BioPharm Ltd — FEI 1000346340

The FDA completed an inspection of Ipsen BioPharm Ltd on July 6, 2018 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
July 6, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wrexham (United Kingdom)