LaMarquise Inc.

FDA Regulatory Profile

LaMarquise Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Apr 3, 2024 · 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 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 3, 2024Upper Arlington, OHFood/CosmeticsNo Action Indicated (NAI)3003174315
Jul 25, 2019Upper Arlington, OHFood/CosmeticsNo Action Indicated (NAI)3003174315
Jun 8, 2018Upper Arlington, OHFood/CosmeticsOfficial Action Indicated (OAI)3003174315
Mar 18, 2015Upper Arlington, OHFood/CosmeticsNo Action Indicated (NAI)3003174315
Sep 10, 2012Upper Arlington, OHFood/CosmeticsNo Action Indicated (NAI)3003174315
Aug 11, 2010Upper Arlington, OHFood/CosmeticsNo Action Indicated (NAI)3003174315

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 3003174315Upper Arlington, OH6Apr 3, 2024

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