FDA Inspection 983531 — Novo Nordisk Inc.

Novo Nordisk Inc. — FEI 2244771

The FDA completed an inspection of Novo Nordisk Inc. on Jul 22, 2016 in Plainsboro, NJ. 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 22, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Plainsboro, NJ (United States)

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