FDA Inspection 1136201 — Novo Nordisk Production Belgium SA

Novo Nordisk Production Belgium SA — FEI 3007647000

The FDA completed an inspection of Novo Nordisk Production Belgium SA on Jan 22, 2020 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
Jan 22, 2020
Fiscal Year
2020
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.