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Sentiar, Inc.

FDA Regulatory Profile

Sentiar, Inc. has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Mar 21, 2024 · VAI
Latest 510(k)
Jul 14, 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) clearances2Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 21, 2024Saint Louis, MODevicesVoluntary Action Indicated (VAI)3017435704

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
K223290CommandEP Data Manager PC (DPC02), CommandEP HMD (HMD02)Jul 14, 2023
K192890SentEPSep 18, 2020

FDA data resources