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Anschel Technology, Inc.

FDA Regulatory Profile

Anschel Technology, Inc. has 0 FDA recalls, 4 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Sep 20, 2022 · NAI
Latest 510(k)
Jun 6, 2012

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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
Inspections4Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 20, 2022Rocky Point, NYDevicesNo Action Indicated (NAI)3010120146
Dec 31, 2019Rocky Point, NYDevicesVoluntary Action Indicated (VAI)3010120146
Aug 16, 2016Rocky Point, NYDevicesVoluntary Action Indicated (VAI)3010120146
Nov 26, 2013Rocky Point, NYDevicesVoluntary Action Indicated (VAI)3010120146

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
K113785ADHERENT VISUAL STIMULATOR GOGGLESJun 6, 2012

FDA data resources