FDA Inspection 1059005 — Ipsen BioPharm Ltd

Ipsen BioPharm Ltd — FEI 1000346340

The FDA completed an inspection of Ipsen BioPharm Ltd on Jul 6, 2018 in Wrexham. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 6, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wrexham (United Kingdom)

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