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Cosmetic Specialty Labs, Inc

FDA Regulatory Profile

Cosmetic Specialty Labs, Inc has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Sep 20, 2023 · OAI

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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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 20, 2023Lawton, OKDrugsOfficial Action Indicated (OAI)1622491
Sep 11, 2015Lawton, OKDrugsVoluntary Action Indicated (VAI)1622491
Nov 26, 2013Lawton, OKDrugsVoluntary Action Indicated (VAI)1622491
Sep 22, 2010Lawton, OKDrugsVoluntary Action Indicated (VAI)1622491
Sep 3, 2009Lawton, OKFood/CosmeticsVoluntary Action Indicated (VAI)1622491

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 1622491Lawton, OK5Sep 20, 2023

FDA data resources

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