FDA Inspection 834355 — Novo Nordisk A/S - Hax

Novo Nordisk A/S - Hax — FEI 3002807748

The FDA completed an inspection of Novo Nordisk A/S - Hax on May 1, 2013 in Gentofte. 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
May 1, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Gentofte (Denmark)