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Morin Enterprises

FDA Regulatory Profile

Morin Enterprises has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
Feb 22, 2023 · 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
Inspections2Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 22, 2023Coon Rapids, MNTobaccoNo Action Indicated (NAI)3013889341
Mar 24, 2022Coon Rapids, MNTobaccoOfficial Action Indicated (OAI)3013889341

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 3013889341Coon Rapids, MN2Feb 22, 2023

FDA data resources

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