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Melaleuca Inc

FDA Regulatory Profile

Melaleuca Inc has 0 FDA recalls, 25 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 8, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections25Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 8, 2025Kansas City, MOFood/CosmeticsNo Action Indicated (NAI)3020788985
Aug 27, 2025Idaho Falls, IDDrugsVoluntary Action Indicated (VAI)3021937
May 14, 2025Knoxville, TNDrugsVoluntary Action Indicated (VAI)1000151121
May 8, 2025Idaho Falls, IDFood/CosmeticsNo Action Indicated (NAI)3022798
May 7, 2025Rexburg, IDFood/CosmeticsNo Action Indicated (NAI)1000307359
Jun 9, 2023Idaho Falls, IDFood/CosmeticsVoluntary Action Indicated (VAI)3022798
Jun 9, 2023Idaho Falls, IDFood/CosmeticsNo Action Indicated (NAI)3022798
Sep 15, 2022Idaho Falls, IDFood/CosmeticsNo Action Indicated (NAI)3017261548
Mar 4, 2022Idaho Falls, IDFood/CosmeticsNo Action Indicated (NAI)3013238472
Aug 9, 2019Idaho Falls, IDDrugsVoluntary Action Indicated (VAI)3021937
May 10, 2019Knoxville, TNDrugsVoluntary Action Indicated (VAI)1000151121
Jan 26, 2017Idaho Falls, IDFood/CosmeticsNo Action Indicated (NAI)3022798
Jan 26, 2017Idaho Falls, IDFood/CosmeticsNo Action Indicated (NAI)3022798
Jan 23, 2017Idaho Falls, IDFood/CosmeticsNo Action Indicated (NAI)3021937
Jan 20, 2017Rexburg, IDFood/CosmeticsNo Action Indicated (NAI)1000307359
Dec 18, 2015Knoxville, TNFood/CosmeticsNo Action Indicated (NAI)1000151121
Aug 28, 2014Knoxville, TNDrugsNo Action Indicated (NAI)1000151121
Nov 8, 2013Idaho Falls, IDDrugsNo Action Indicated (NAI)3021937
Mar 6, 2012Knoxville, TNDrugsVoluntary Action Indicated (VAI)1000151121
Nov 2, 2011Idaho Falls, IDDrugsVoluntary Action Indicated (VAI)3021937

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.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3020788985Kansas City, MO1Oct 8, 2025
FEI 3021937Idaho Falls, ID7Aug 27, 2025
FEI 1000151121Knoxville, TN6May 14, 2025
FEI 3022798Idaho Falls, ID7May 8, 2025
FEI 1000307359Rexburg, ID2May 7, 2025
FEI 3017261548Idaho Falls, ID1Sep 15, 2022
FEI 3013238472Idaho Falls, ID1Mar 4, 2022

FDA data resources

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