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Harbor Marine Product Inc., a seafood processor and importer in Vernon, California, was cited for serious violations of seafood safety regulations during an FDA inspection from March 5-27, 2025. The FDA found that the company's raw, ready-to-eat fish products were adulterated due to preparation under insanitary conditions, with environmental testing detecting non-pathogenic Listeria spp. in samples collected from the processing facility. The company failed to develop and implement a compliant Hazard Analysis and Critical Control Point (HACCP) plan as required under 21 CFR Part 123, and as an importer, failed to obtain adequate assurances that imported fish products met U.S. processing safety standards.