Meiko Food Co. Inc.

FDA Regulatory Profile

Meiko Food Co. Inc. has 4 FDA recalls, 9 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest recall
F-1804-2012 · Class II · Jul 16, 2012
Latest inspection
Aug 20, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls4Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections9Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-1804-2012Class IIMeiko Foods Co. Inc. Cooked Cuttlefish Ball, 2-10 lb bags . Product labeling reads in part:"…Jul 16, 2012
F-1802-2012Class IIMeiko Foods Co. Inc. Tempura, 12 oz. Product labeling reads in part:" MEIKO***TEMPURA ***MEIKO FOODS…Jul 16, 2012
F-1803-2012Class IIMeiko Foods Co. Inc. Pollock Fish Balls , 2-10 lb bags. Product labeling reads in part:"…Jul 16, 2012
F-1801-2012Class IIMeiko Foods Co. Inc. Cooked Shrimp Balls, 8 oz. Product labeling reads in part:" TOM VIEN COOKED…Jul 16, 2012

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 20, 2025South El Monte, CAFood/CosmeticsNo Action Indicated (NAI)3001452191
Nov 9, 2021South El Monte, CAFood/CosmeticsNo Action Indicated (NAI)3001452191
Dec 7, 2018South El Monte, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001452191
Jan 14, 2016South El Monte, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001452191
Apr 11, 2013South El Monte, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001452191
Jul 17, 2012South El Monte, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001452191
Jul 10, 2012South El Monte, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001452191
May 19, 2011South El Monte, CAFood/CosmeticsOfficial Action Indicated (OAI)3001452191
Aug 19, 2010South El Monte, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001452191

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 3001452191South El Monte, CA9Aug 20, 2025

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