FDA Inspection 710676 — Octapharma AB

Octapharma AB — FEI 3005559915

The FDA completed an inspection of Octapharma AB on Jan 20, 2011 in Stockholm. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Biologics.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Jan 20, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Stockholm (Sweden)

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