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Dowell Dental Products Inc

FDA Regulatory Profile

Dowell Dental Products Inc has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 13, 2025 · VAI

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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
Inspections4Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 13, 2025Rancho Cucamonga, CABiologicsVoluntary Action Indicated (VAI)3006769505
Nov 16, 2018Rancho Cucamonga, CABiologicsNo Action Indicated (NAI)3006769505
Apr 1, 2015Rancho Cucamonga, CABiologicsNo Action Indicated (NAI)3006769505
Apr 5, 2010Rancho Cucamonga, CADevicesNo Action Indicated (NAI)3006769505

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 3006769505Rancho Cucamonga, CA4Jun 13, 2025

FDA data resources

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