Iq Technologies, Inc.

FDA Regulatory Profile

Iq Technologies, Inc. has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jan 10, 2023 · NAI
Latest 510(k)
May 26, 2017

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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) clearances2Oct 4, 2026Not statedCurrent
Inspections3Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 10, 2023Las Vegas, NVDevicesNo Action Indicated (NAI)3008806536
Dec 12, 2017Las Vegas, NVDevicesNo Action Indicated (NAI)3008806536
Jan 24, 2014Las Vegas, NVDevicesVoluntary Action Indicated (VAI)3008806536

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
K170659IQ TechnologiesMay 26, 2017
K131290IQ TECHNOLOGIESAug 6, 2014