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Altaravision, Inc.

FDA Regulatory Profile

Altaravision, Inc. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Mar 20, 2018 · NAI
Latest 510(k)
Apr 15, 2019

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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 20, 2018Apex, NCDevicesNo Action Indicated (NAI)3008774169
May 13, 2015Apex, NCDevicesNo Action Indicated (NAI)3008774169

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
K190420NDOHD High Definition Imaging System (NDOHD)Apr 15, 2019

FDA data resources