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FDA Inspection 981954 — Sandoz Incorporated

Sandoz Incorporated — FEI 1717759

The FDA completed an inspection of Sandoz Incorporated on October 30, 2015 in East Hanover, NJ. 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
October 30, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
East Hanover, NJ (United States)

Facility

Other inspections at this facility

  • 1087173 (VAI Tue Apr 16 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1013036 (NAI Wed Mar 29 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 853190 (VAI Thu Oct 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 797878 (VAI Tue Aug 14 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 727431 (OAI Fri May 06 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources