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FDA Inspection 902814 — 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 7, 2014 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 7, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Athlone (Ireland)

Facility

Other inspections at this facility

  • 1205233 (NAI Wed Apr 05 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1202701 (VAI Fri Oct 28 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1043417 (NAI Thu Jan 25 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 993675 (NAI Fri Nov 18 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 802376 (NAI Fri Sep 07 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources