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Arthrex Inland Empire

FDA Regulatory Profile

Arthrex Inland Empire has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 6, 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
Inspections5Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 6, 2025Corona, CABiologicsNo Action Indicated (NAI)3006228878
Aug 24, 2018Corona, CABiologicsVoluntary Action Indicated (VAI)3006228878
Jun 22, 2016Corona, CABiologicsNo Action Indicated (NAI)3006228878
Oct 16, 2012Corona, CABiologicsNo Action Indicated (NAI)3006228878
Nov 25, 2009Corona, CABiologicsVoluntary Action Indicated (VAI)3006228878

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 3006228878Corona, CA5Aug 6, 2025

FDA data resources

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