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OPMX, LLC

FEI 3008937007 · 333 H St Ste 5000, Chula Vista, California, 91910, United States

1 warning letter on record

Per FDA, as of 2026-10-31 · Sources: FDA Data Dashboard, Import Alerts, Enforcement Reports

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Import alerts
0
Import refusals (5 years)
0
Warning letters
1
Last FDA action
2026-09-24
38 days ago

FDA record

  1. 2026-09-24
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  2. 2024-12-10
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  3. 2023-07-07
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  4. 2023-07-07
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  5. 2013-02-20
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  6. 2011-10-11
    Warning letterFDA Warning Letter (CFSAN)
    FDA source
  7. 2011-05-31
    RecallRecall F-1378-2011 · Class 2 · This recall of PENTREXCILINA was initiated after an FDA inspection revealed that several products were being distributed with packaging that may have been mistakenly confused with the PENTREXYL antibiotics readily available in Mexico and possibly familiar to Hispanic consumers.
    Pentrexcilina citricillin 500 Dietary supplement capsules with herbs
    Source: FDA Enforcement Reports
  8. 2011-05-31
    InspectionFDA inspection · Classification: Official Action Indicated (OAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source