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FDA Inspection 589462 — Dixie Dew Products Inc

Dixie Dew Products Inc — FEI 1022121

The FDA completed an inspection of Dixie Dew Products Inc on June 15, 2009 in Erlanger, KY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 15, 2009
Fiscal Year
2009
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Erlanger, KY (United States)

Facility

Other inspections at this facility

  • 1032243 (OAI Thu Oct 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1032242 (OAI Tue Sep 26 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1015991 (OAI Wed Jun 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1010712 (OAI Thu Apr 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1000596 (NAI Tue Feb 07 2017 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources