FDA Inspection 993675 — Novo Nordisk Production Ireland Limited

Novo Nordisk Production Ireland Limited — FEI 3002806873

The FDA completed an inspection of Novo Nordisk Production Ireland Limited on November 18, 2016 in Athlone. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 18, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Athlone (Ireland)