FDA Inspection 1246550 — Novo Nordisk Production Belgium SA

Novo Nordisk Production Belgium SA — FEI 3007647000

The FDA completed an inspection of Novo Nordisk Production Belgium SA on Apr 7, 2023 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: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 7, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brussels (Belgium)

Additional details

Mutual Recognition Agreement (MRA)

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