FDA Inspection 730949 — Novo Nordisk A/S

Novo Nordisk A/S — FEI 3002807751

The FDA completed an inspection of Novo Nordisk A/S on February 8, 2011 in Kalundborg. 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
February 8, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kalundborg (Denmark)