FDA Inspection 1007260 — Novo Nordisk A/S

Novo Nordisk A/S — FEI 3000151819

The FDA completed an inspection of Novo Nordisk A/S on Feb 8, 2017 in Bagsvard. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 8, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bagsvard (Denmark)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.