AQUABEST SEAFOOD LLC

FDA Regulatory Profile

AQUABEST SEAFOOD LLC has 3 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
F-0524-2020 · Class II · Nov 26, 2019
Latest inspection
Jul 22, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls3Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-0524-2020Class IISea Mart Frozen Yellowfin Tuna Loin, CO treated, skinless, boneless, bloodline removed, center cut…Nov 26, 2019
F-0525-2020Class IISea Mart Frozen Yellowfin Tuna Saku, CO treated, skinless, boneless, bloodline removed, 10-12oz, 10…Nov 26, 2019
F-0523-2020Class IISea Mart Frozen Yellowfin Tuna Steak, CO treated, skinless, boneless, bloodline removed, 8 oz, 10lb…Nov 26, 2019

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 22, 2025Miami, FLFood/CosmeticsVoluntary Action Indicated (VAI)3007890228
Nov 8, 2021Miami, FLFood/CosmeticsNo Action Indicated (NAI)3007890228

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3007890228Miami, FL2Jul 22, 2025

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.