Lantmannen Unibake USA Inc.,

FDA Regulatory Profile

Lantmannen Unibake USA Inc., has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 7, 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
Inspections6Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 7, 2025Saint Petersburg, FLFood/CosmeticsNo Action Indicated (NAI)3006381063
Sep 13, 2023Saint Petersburg, FLFood/CosmeticsNo Action Indicated (NAI)3006381063
Mar 17, 2021Lisle, ILFood/CosmeticsNo Action Indicated (NAI)3009135717
Nov 5, 2018Lisle, ILFood/CosmeticsVoluntary Action Indicated (VAI)3009135717
Apr 17, 2018Saint Petersburg, FLFood/CosmeticsNo Action Indicated (NAI)3006381063
May 9, 2011Saint Petersburg, FLFood/CosmeticsVoluntary Action Indicated (VAI)3006381063

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 3006381063Saint Petersburg, FL4Aug 7, 2025
FEI 3009135717Lisle, IL2Mar 17, 2021

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