Versiti Illinois Inc

FDA Regulatory Profile

Versiti Illinois Inc has 0 FDA recalls, 82 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 24, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections82Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 24, 2025Westmont, ILBiologicsNo Action Indicated (NAI)1000115106
Jan 29, 2025Dekalb, ILBiologicsNo Action Indicated (NAI)3005010959
Jan 16, 2025Aurora, ILBiologicsNo Action Indicated (NAI)1470274
Nov 18, 2024Chicago, ILBiologicsNo Action Indicated (NAI)3009775812
Nov 6, 2024Bloomingdale, ILBiologicsNo Action Indicated (NAI)3008393297
Aug 2, 2024Crystal Lake, ILBiologicsNo Action Indicated (NAI)3000206204
Jun 13, 2024Tinley Park, ILBiologicsNo Action Indicated (NAI)1470340
Mar 14, 2024Highland, INBiologicsNo Action Indicated (NAI)1000115640
Feb 6, 2023Geneva, ILBiologicsNo Action Indicated (NAI)3003922327
Sep 15, 2022Aurora, ILBiologicsNo Action Indicated (NAI)1470274
May 24, 2022Westmont, ILBiologicsNo Action Indicated (NAI)1000115106
Mar 24, 2022Joliet, ILBiologicsNo Action Indicated (NAI)1470337
Mar 22, 2022Elgin, ILBiologicsNo Action Indicated (NAI)1471716
Sep 17, 2019Dekalb, ILBiologicsNo Action Indicated (NAI)3005010959
Sep 17, 2019Bloomingdale, ILBiologicsNo Action Indicated (NAI)3008393297
Aug 12, 2019Tinley Park, ILBiologicsVoluntary Action Indicated (VAI)1470340
May 8, 2019Chicago, ILBiologicsNo Action Indicated (NAI)3009775812
Dec 18, 2018Geneva, ILBiologicsNo Action Indicated (NAI)3003922327
Oct 22, 2018Crystal Lake, ILBiologicsNo Action Indicated (NAI)3000206204
Jul 9, 2018Joliet, ILBiologicsNo Action Indicated (NAI)1470337

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 1000115106Westmont, IL6Jun 24, 2025
FEI 3005010959Dekalb, IL7Jan 29, 2025
FEI 1470274Aurora, IL8Jan 16, 2025
FEI 3009775812Chicago, IL2Nov 18, 2024
FEI 3008393297Bloomingdale, IL6Nov 6, 2024
FEI 3000206204Crystal Lake, IL7Aug 2, 2024
FEI 1470340Tinley Park, IL7Jun 13, 2024
FEI 1000115640Highland, IN7Mar 14, 2024
FEI 3003922327Geneva, IL7Feb 6, 2023
FEI 1470337Joliet, IL6Mar 24, 2022
FEI 1471716Elgin, IL6Mar 22, 2022
FEI 3006041278Plainfield, IL5Dec 22, 2015
FEI 3007047814Saint Charles, IL3Nov 5, 2013
FEI 3006523757Frankfort, IL2Jun 25, 2012
FEI 3007477714Morris, IL2Feb 15, 2012
FEI 3005240626Schaumburg, IL1Jan 9, 2010

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.