Eurofins Viracor, LLC.

FDA Regulatory Profile

Eurofins Viracor, LLC. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 16, 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 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 16, 2025Lenexa, KSDevicesNo Action Indicated (NAI)3005651716
Apr 19, 2023Lenexa, KSDevicesNo Action Indicated (NAI)3005651716
Jul 26, 2019Lenexa, KSDevicesVoluntary Action Indicated (VAI)3005651716
Sep 19, 2018Lenexa, KSBiologicsNo Action Indicated (NAI)3005651716
Sep 2, 2016Lenexa, KSBiologicsNo Action Indicated (NAI)3005651716
Apr 24, 2014Lenexa, KSDevicesNo Action Indicated (NAI)3005651716
Jul 8, 2010Lenexa, KSDevicesNo Action Indicated (NAI)3005651716

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 3005651716Lenexa, KS7Sep 16, 2025

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