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Herbalife International

FDA Regulatory Profile

Herbalife International has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 10, 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
Inspections3Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 10, 2025Houston, TXFood/CosmeticsNo Action Indicated (NAI)3010012594
Apr 16, 2024Doral, FLFood/CosmeticsVoluntary Action Indicated (VAI)3013025746
Mar 21, 2023Bronx, NYFood/CosmeticsNo Action Indicated (NAI)3010012588

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 3010012594Houston, TX1Jul 10, 2025
FEI 3013025746Doral, FL1Apr 16, 2024
FEI 3010012588Bronx, NY1Mar 21, 2023

FDA data resources

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