FDA Inspection 1026864 — ALTEX USA CORPORATION

ALTEX USA CORPORATION — FEI 3012778618

The FDA completed an inspection of ALTEX USA CORPORATION on September 21, 2017 in Miami, FL. 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
September 21, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Miami, FL (United States)

Additional Details

FSVP