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Radialogica, LLC

FDA Regulatory Profile

Radialogica, LLC has 0 FDA recalls, 3 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Mar 6, 2024 · NAI
Latest 510(k)
Apr 4, 2018

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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
Inspections3Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 6, 2024Saint Louis, MODevicesNo Action Indicated (NAI)3009140718
Jan 19, 2018Saint Louis, MODevicesNo Action Indicated (NAI)3009140718
Jan 15, 2015Saint Louis, MODevicesNo Action Indicated (NAI)3009140718

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
K180595SciMoCaApr 4, 2018

FDA data resources