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FDA Inspection 793700 — Novo Nordisk A/S - Hax

Novo Nordisk A/S - Hax — FEI 3002807748

The FDA completed an inspection of Novo Nordisk A/S - Hax on June 26, 2012 in Gentofte. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 26, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gentofte (Denmark)

Facility

Other inspections at this facility

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  • 1056878 (NAI Tue May 08 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 985214 (NAI Tue Jun 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 950758 (VAI Fri Nov 06 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 883249 (VAI Tue May 13 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources