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CLW LLC

FDA Regulatory Profile

CLW LLC has 0 FDA recalls, 10 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 13, 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
Inspections10Nov 12, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 13, 2025Lawton, OKFood/CosmeticsNo Action Indicated (NAI)1000117634
Mar 16, 2022Lawton, OKFood/CosmeticsVoluntary Action Indicated (VAI)1000117634
Feb 6, 2018Lawton, OKFood/CosmeticsNo Action Indicated (NAI)1000117634
Jul 11, 2017Lawton, OKFood/CosmeticsVoluntary Action Indicated (VAI)1000117634
Jul 15, 2014Lawton, OKFood/CosmeticsVoluntary Action Indicated (VAI)1000117634
Aug 15, 2012Lawton, OKFood/CosmeticsNo Action Indicated (NAI)1000117634
Nov 30, 2011Lawton, OKFood/CosmeticsNo Action Indicated (NAI)1000117634
Jan 6, 2011Lawton, OKFood/CosmeticsVoluntary Action Indicated (VAI)1000117634
May 26, 2010Lawton, OKFood/CosmeticsVoluntary Action Indicated (VAI)1000117634
Sep 11, 2009Lawton, OKFood/CosmeticsVoluntary Action Indicated (VAI)1000117634

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 1000117634Lawton, OK10May 13, 2025

FDA data resources

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