Crevel Distribution Inc.

FDA Regulatory Profile

Crevel Distribution Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jul 24, 2026 · 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
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 24, 2026Hanover, MDFood/CosmeticsNo Action Indicated (NAI)3012377275
Oct 30, 2025Hanover, MDFood/CosmeticsOfficial Action Indicated (OAI)3012377275
Jun 23, 2023Hanover, MDFood/CosmeticsVoluntary Action Indicated (VAI)3012377275
Jun 8, 2022Hanover, MDFood/CosmeticsVoluntary Action Indicated (VAI)3012377275
Aug 25, 2020Hanover, MDFood/CosmeticsVoluntary Action Indicated (VAI)3012377275
May 10, 2018Hanover, MDFood/CosmeticsVoluntary Action Indicated (VAI)3012377275

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 3012377275Hanover, MD6Jul 24, 2026

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