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Laboratorios Liomont, S.A. De C.V.

FDA Regulatory Profile

Laboratorios Liomont, S.A. De C.V. has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 4, 2023 · 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
Inspections3Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 4, 2023Ciudad De Mexico, MexicoDrugsVoluntary Action Indicated (VAI)3003948827
Dec 15, 2017Ciudad De Mexico, MexicoDrugsNo Action Indicated (NAI)3003948827
Oct 19, 2012Ciudad De Mexico, MexicoDrugsNo Action Indicated (NAI)3003948827

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 3003948827Ciudad De Mexico, Mexico3Aug 4, 2023

FDA data resources

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