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Mriglobal

FDA Regulatory Profile

Mriglobal has 0 FDA recalls, 7 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Aug 29, 2022 · VAI
Latest 510(k)
Oct 1, 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) clearances1Oct 4, 2026Not statedCurrent
Inspections7Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 29, 2022Kansas City, MODrugsVoluntary Action Indicated (VAI)1917659
Aug 26, 2022North Kansas City, MODrugsNo Action Indicated (NAI)3009563664
Nov 7, 2016North Kansas City, MODrugsNo Action Indicated (NAI)3009563664
Nov 7, 2016Kansas City, MODrugsNo Action Indicated (NAI)1917659
May 22, 2012Kansas City, MODrugsVoluntary Action Indicated (VAI)1917659
May 21, 2012North Kansas City, MODrugsNo Action Indicated (NAI)3009563664
Jul 17, 2009Kansas City, MODrugsNo Action Indicated (NAI)1917659

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
K183462Applied Biosystems Bacillus anthracis Detection KitOct 1, 2019

FDA data resources