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Visura Technologies, LLC

FDA Regulatory Profile

Visura Technologies, LLC has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Mar 24, 2026 · VAI
Latest 510(k)
Jun 20, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances1Oct 4, 2026Not statedCurrent
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 24, 2026Minneapolis, MNDevicesVoluntary Action Indicated (VAI)3015194986
Nov 5, 2019Minneapolis, MNDevicesNo Action Indicated (NAI)3015194986

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.

Recent 510(k) Clearances

K-NumberDeviceDate
K180911Visura Technologies TEECAD SystemJun 20, 2018

FDA data resources