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J Deluca Fish Company, Inc.

FDA Regulatory Profile

J Deluca Fish Company, Inc. has 0 FDA recalls, 17 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Sep 19, 2025 · NAI

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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
Inspections17Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 19, 2025Wilmington, CAFood/CosmeticsNo Action Indicated (NAI)1000125710
Aug 28, 2025San Pedro, CAFood/CosmeticsNo Action Indicated (NAI)2000020287
May 13, 2021Wilmington, CAFood/CosmeticsNo Action Indicated (NAI)1000125710
May 11, 2021San Pedro, CAFood/CosmeticsVoluntary Action Indicated (VAI)2000020287
Sep 7, 2018Wilmington, CAFood/CosmeticsNo Action Indicated (NAI)1000125710
Sep 5, 2018San Pedro, CAFood/CosmeticsNo Action Indicated (NAI)2000020287
Aug 31, 2015Wilmington, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000125710
Aug 31, 2015San Pedro, CAFood/CosmeticsVoluntary Action Indicated (VAI)2000020287
Jul 10, 2014San Pedro, CAFood/CosmeticsVoluntary Action Indicated (VAI)2000020287
Jun 6, 2013Wilmington, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000125710
Jun 6, 2013Wilmington, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000125710
Mar 18, 2013Vernon, CAFood/CosmeticsVoluntary Action Indicated (VAI)3009737992
Sep 1, 2011San Pedro, CAFood/CosmeticsOfficial Action Indicated (OAI)2000020287
Nov 28, 2010Wilmington, CAFood/CosmeticsNo Action Indicated (NAI)1000125710
Aug 23, 2010Wilmington, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000125710
Jul 1, 2010San Pedro, CAFood/CosmeticsVoluntary Action Indicated (VAI)2000020287
Jul 23, 2009San Pedro, CAFood/CosmeticsVoluntary Action Indicated (VAI)2000020287

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 1000125710Wilmington, CA8Sep 19, 2025
FEI 2000020287San Pedro, CA8Aug 28, 2025
FEI 3009737992Vernon, CA1Mar 18, 2013

FDA data resources

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