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FDA Inspection 855726 — Fagron, Inc

Fagron, Inc — FEI 1000174332

The FDA completed an inspection of Fagron, Inc on November 18, 2013 in Saint Paul, MN. 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
November 18, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Paul, MN (United States)

Facility

Other inspections at this facility

  • 1156943 (OAI Thu Nov 18 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1085788 (VAI Wed Apr 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1035676 (OAI Thu Dec 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 949588 (VAI Tue Nov 10 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 924881 (VAI Wed Apr 29 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources