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Midwest Sterilization Corporation

FDA Regulatory Profile

Midwest Sterilization Corporation has 0 FDA recalls, 11 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Mar 21, 2024 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections11Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 21, 2024Laredo, TXDevicesNo Action Indicated (NAI)3005012805
Feb 16, 2024Jackson, MODevicesVoluntary Action Indicated (VAI)1928237
Jan 12, 2023Laredo, TXDevicesOfficial Action Indicated (OAI)3005012805
Nov 10, 2022Jackson, MODevicesOfficial Action Indicated (OAI)1928237
Sep 2, 2021Jackson, MODevicesOfficial Action Indicated (OAI)1928237
Nov 7, 2018Jackson, MODevicesVoluntary Action Indicated (VAI)1928237
Mar 22, 2018Jackson, MODevicesVoluntary Action Indicated (VAI)1928237
Jun 18, 2015Jackson, MODevicesVoluntary Action Indicated (VAI)1928237
Mar 28, 2013Laredo, TXDevicesNo Action Indicated (NAI)3005012805
Feb 12, 2013Jackson, MODevicesNo Action Indicated (NAI)1928237
Dec 13, 2010Jackson, MODevicesNo Action Indicated (NAI)1928237

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 3005012805Laredo, TX3Mar 21, 2024
FEI 1928237Jackson, MO8Feb 16, 2024

FDA data resources

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