Versiti Wisconsin, Inc

FDA Regulatory Profile

Versiti Wisconsin, Inc has 0 FDA recalls, 76 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 17, 2026 · 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
Inspections76Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 17, 2026Milwaukee, WIBiologicsNo Action Indicated (NAI)2171378
Jun 26, 2025Manitowoc, WIBiologicsNo Action Indicated (NAI)1000520116
Jun 12, 2025Mount Pleasant, WIBiologicsNo Action Indicated (NAI)2177744
Apr 16, 2025La Crosse, WIBiologicsNo Action Indicated (NAI)3004038411
Jul 11, 2024Kenosha, WIBiologicsNo Action Indicated (NAI)2177740
Apr 30, 2024Marshfield, WIBiologicsNo Action Indicated (NAI)3000717959
Apr 22, 2024West Bend, WIBiologicsNo Action Indicated (NAI)1000116313
Apr 22, 2024Waukesha, WIBiologicsNo Action Indicated (NAI)2177747
Apr 19, 2024Wauwatosa, WIBiologicsNo Action Indicated (NAI)1000116289
Mar 4, 2024Milwaukee, WIBiologicsNo Action Indicated (NAI)2171378
Aug 24, 2023Manitowoc, WIBiologicsNo Action Indicated (NAI)1000520116
Apr 26, 2023Milwaukee, WIBiologicsNo Action Indicated (NAI)2171378
Dec 13, 2022Mount Pleasant, WIBiologicsNo Action Indicated (NAI)2177744
Dec 13, 2019Milwaukee, WIBiologicsNo Action Indicated (NAI)2171378
Dec 11, 2019Marshfield, WIBiologicsNo Action Indicated (NAI)3000717959
Oct 30, 2019La Crosse, WIBiologicsNo Action Indicated (NAI)3004038411
Mar 22, 2019Wauwatosa, WIBiologicsNo Action Indicated (NAI)1000116289
Mar 20, 2019West Bend, WIBiologicsNo Action Indicated (NAI)1000116313
Mar 19, 2019Waukesha, WIBiologicsNo Action Indicated (NAI)2177747
Sep 25, 2018Kenosha, WIBiologicsNo Action Indicated (NAI)2177740

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 2171378Milwaukee, WI15Jul 17, 2026
FEI 1000520116Manitowoc, WI7Jun 26, 2025
FEI 2177744Mount Pleasant, WI7Jun 12, 2025
FEI 3004038411La Crosse, WI7Apr 16, 2025
FEI 2177740Kenosha, WI6Jul 11, 2024
FEI 3000717959Marshfield, WI7Apr 30, 2024
FEI 1000116313West Bend, WI7Apr 22, 2024
FEI 2177747Waukesha, WI7Apr 22, 2024
FEI 1000116289Wauwatosa, WI7Apr 19, 2024
FEI 3002860769Fitchburg, WI6May 31, 2018

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