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Action Labs, Inc

FEI 3003520044 · 813 Towne Center Dr, Pomona, California, 91767, United States

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
0
Last FDA action
2021-07-01
5 years ago

FDA record

  1. 2021-07-01
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  2. 2021-07-01
    InspectionFDA inspection · Classification: No Action Indicated (NAI)
    Project area: Foodborne Biological Hazards
    FDA source
  3. 2013-12-06
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  4. 2012-07-17
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Food Composition, Standards, Labeling and Econ
    FDA source
  5. 2012-07-17
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Foodborne Biological Hazards
    FDA source
  6. 2007-05-23
    RecallRecall F-449-7 · Class 1 · Testing performed recently at NBTY, Inc. (the manufacturer) shows that the recalled capsules have the potential to be contaminated with Salmonella. Although multiple lot numbers may have been involved in the recall by NBTY, only NBTY lot number 64951 was purchased, repacked and distributed by Action Labs, Inc.
    Sentinel Shark Cartilage 750mg, lot number 064951, expiration date 07 2009, UPC 28245 00313 6
    Source: FDA Enforcement Reports