FDA Inspection 574834 — Novo Nordisk A/S

Novo Nordisk A/S — FEI 3002807751

The FDA completed an inspection of Novo Nordisk A/S on February 24, 2009 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 24, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Kalundborg (Denmark)