Maruhide Marine Products Inc

FDA Regulatory Profile

Maruhide Marine Products Inc has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 31, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections7Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 31, 2025Long Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)2027674
Mar 25, 2022Long Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)2027674
Apr 18, 2019Long Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)2027674
May 11, 2016Long Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)2027674
Oct 29, 2014Long Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)2027674
Dec 6, 2012Long Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)2027674
May 4, 2010Long Beach, CAFood/CosmeticsVoluntary Action Indicated (VAI)2027674

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 2027674Long Beach, CA7Jul 31, 2025

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