Lamb Weston Holdings, Inc

FDA Regulatory Profile

Lamb Weston Holdings, Inc has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 13, 2026 · 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
Inspections8Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 13, 2026Eagle, IDFood/CosmeticsNo Action Indicated (NAI)3004289553
Jun 10, 2025American Falls, IDFood/CosmeticsNo Action Indicated (NAI)3016292
May 2, 2022American Falls, IDFood/CosmeticsNo Action Indicated (NAI)3016292
Nov 17, 2021Eagle, IDFood/CosmeticsNo Action Indicated (NAI)3004289553
Jun 27, 2017American Falls, IDFood/CosmeticsNo Action Indicated (NAI)3016292
Feb 25, 2015American Falls, IDFood/CosmeticsNo Action Indicated (NAI)3016292
Jul 6, 2010American Falls, IDFood/CosmeticsNo Action Indicated (NAI)3016292
Jun 1, 2009American Falls, IDFood/CosmeticsNo Action Indicated (NAI)3016292

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 3004289553Eagle, ID2Jul 13, 2026
FEI 3016292American Falls, ID6Jun 10, 2025

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