FDA Inspection 734988 — Novo Nordisk Production Belgium SA

Novo Nordisk Production Belgium SA — FEI 3007647000

The FDA completed an inspection of Novo Nordisk Production Belgium SA on Jun 10, 2011 in Brussels. 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
Jun 10, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Brussels (Belgium)

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