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Cnsystems Medizintechnik GmbH

FDA Regulatory Profile

Cnsystems Medizintechnik GmbH has 0 FDA recalls, 2 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 11, 2017 · NAI
Latest 510(k)
Apr 12, 2023

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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) clearances3Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
May 11, 2017Graz, AustriaDevicesNo Action Indicated (NAI)3006113127
Sep 27, 2012Graz, AustriaDevicesVoluntary Action Indicated (VAI)3006113127

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
K223332Task Force COREApr 12, 2023
K183521CNAP MonitorSep 11, 2019
K014063TASK FORCE MONITOR 3040Feb 7, 2002

FDA data resources