FDA Inspection 806442 — Xellia Pharmaceuticals ApS

Xellia Pharmaceuticals ApS — FEI 3002806860

The FDA completed an inspection of Xellia Pharmaceuticals ApS on October 16, 2012 in Copenhagen S. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 16, 2012
Fiscal Year
2013
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Copenhagen S (Denmark)