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FDA Inspection 604502 — MaxPax, LLC

MaxPax, LLC — FEI 2130094

The FDA completed an inspection of MaxPax, LLC on August 14, 2009 in Elkhorn, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 14, 2009
Fiscal Year
2009
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Elkhorn, WI (United States)

Facility

Other inspections at this facility

  • 1097437 (VAI Thu Jul 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 931181 (VAI Wed Jun 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 885213 (VAI Fri Jul 11 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 814003 (VAI Mon Jan 14 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 752375 (VAI Mon Oct 31 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources