Quality Chemical Laboratories

FDA Regulatory Profile

Quality Chemical Laboratories has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 24, 2025 · 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
Inspections7Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 24, 2025Wilmington, NCBiologicsNo Action Indicated (NAI)3002323490
Nov 20, 2024Wilmington, NCDrugsVoluntary Action Indicated (VAI)3002323490
Jul 27, 2017Wilmington, NCDrugsVoluntary Action Indicated (VAI)3002323490
Jun 21, 2016Wilmington, NCVeterinaryNo Action Indicated (NAI)3002323490
Sep 26, 2013Wilmington, NCDrugsVoluntary Action Indicated (VAI)3002323490
Aug 24, 2010Wilmington, NCDrugsVoluntary Action Indicated (VAI)3002323490
Apr 1, 2010Wilmington, NCDrugsNo Action Indicated (NAI)3002323490

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 3002323490Wilmington, NC7Jul 24, 2025

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