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FDA Inspection 1061068 — Novo Nordisk Production Belgium SA

Novo Nordisk Production Belgium SA — FEI 3007647000

The FDA completed an inspection of Novo Nordisk Production Belgium SA on Jul 31, 2018 in Brussels. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 31, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Brussels (Belgium)

Facility

Other inspections at this facility

FDA data resources

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