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Day-Lee Foods, Inc.

FDA Regulatory Profile

Day-Lee Foods, Inc. has 0 FDA recalls, 17 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 29, 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
Inspections17Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 29, 2025Seatac, WAFood/CosmeticsVoluntary Action Indicated (VAI)3012939385
Jun 27, 2025Union City, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003096256
May 15, 2024Santa Fe Springs, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003423835
May 25, 2023Santa Fe Springs, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000303395
Nov 19, 2021Seatac, WAFood/CosmeticsVoluntary Action Indicated (VAI)3012939385
Jun 16, 2020Santa Fe Springs, CAFood/CosmeticsNo Action Indicated (NAI)3003423835
Aug 21, 2019Union City, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003096256
Aug 15, 2019Santa Fe Springs, CAFood/CosmeticsNo Action Indicated (NAI)1000303395
Apr 30, 2018Santa Fe Springs, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003423835
May 4, 2017Santa Fe Springs, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000303395
Nov 20, 2015Santa Fe Springs, CAFood/CosmeticsNo Action Indicated (NAI)1000303395
Aug 20, 2013Union City, CAFood/CosmeticsVoluntary Action Indicated (VAI)3003096256
Jun 19, 2012Santa Fe Springs, CAVeterinaryNo Action Indicated (NAI)1000303395
Aug 25, 2011Santa Fe Springs, CAFood/CosmeticsNo Action Indicated (NAI)1000303395
Mar 9, 2011Santa Fe Springs, CAFood/CosmeticsNo Action Indicated (NAI)1000303395
Oct 12, 2010Santa Fe Springs, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000303395
Sep 8, 2010Santa Fe Springs, CAFood/CosmeticsVoluntary Action Indicated (VAI)1000303395

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 3012939385Seatac, WA2Sep 29, 2025
FEI 3003096256Union City, CA3Jun 27, 2025
FEI 3003423835Santa Fe Springs, CA3May 15, 2024
FEI 1000303395Santa Fe Springs, CA9May 25, 2023

FDA data resources

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