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FDA Inspection 554056 — Vita Plus Corp.

Vita Plus Corp. — FEI 2124202

The FDA completed an inspection of Vita Plus Corp. on December 30, 2008 in Columbus, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 30, 2008
Fiscal Year
2009
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Columbus, WI (United States)

Facility

Other inspections at this facility

  • 1075002 (NAI Thu Dec 06 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1012584 (NAI Mon May 08 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 867066 (NAI Wed Feb 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 767862 (NAI Fri Jan 27 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 702898 (NAI Wed Dec 22 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources