FDA Inspection 983531 — Novo Nordisk Inc.

Novo Nordisk Inc. — FEI 2244771

The FDA completed an inspection of Novo Nordisk Inc. on July 22, 2016 in Plainsboro, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 22, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Plainsboro, NJ (United States)