Malteurop North America Inc.

FDA Regulatory Profile

Malteurop North America Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 14, 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 14, 2025Great Falls, MTFood/CosmeticsNo Action Indicated (NAI)3005381686
Aug 16, 2019Great Falls, MTFood/CosmeticsNo Action Indicated (NAI)3005381686
May 16, 2019Milwaukee, WIFood/CosmeticsNo Action Indicated (NAI)2122273
Sep 19, 2014Great Falls, MTFood/CosmeticsNo Action Indicated (NAI)3005381686
Sep 27, 2012Milwaukee, WIFood/CosmeticsNo Action Indicated (NAI)2122273
Apr 14, 2011Winona, MNVeterinaryNo Action Indicated (NAI)2116182

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 3005381686Great Falls, MT3Aug 14, 2025
FEI 2122273Milwaukee, WI2May 16, 2019
FEI 2116182Winona, MN1Apr 14, 2011

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