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Rudolf Riester GmbH

FDA Regulatory Profile

Rudolf Riester GmbH has 0 FDA recalls, 1 inspection, 3 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 24, 2010 · VAI
Latest 510(k)
Jun 24, 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) clearances3Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 24, 2010Jungingen, GermanyDevicesVoluntary Action Indicated (VAI)1000292048

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
K190927Oscillometric Blood Pressure MonitorJun 24, 2019
K170538RVS-100 Vital Signs MonitorOct 17, 2017
K171182ri-former Predictive ThermometerOct 4, 2017

FDA data resources