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FDA Inspection 1090146 — Intermex Products USA, Ltd

Intermex Products USA, Ltd — FEI 1640978

The FDA completed an inspection of Intermex Products USA, Ltd on May 8, 2019 in Grand Prairie, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 8, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Grand Prairie, TX (United States)

Facility

Other inspections at this facility

  • 1310136 (NAI Wed Mar 11 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1164967 (NAI Tue Feb 22 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 966881 (NAI Fri Apr 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 831102 (VAI Fri May 03 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 545828 (NAI Thu Oct 16 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources