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Schuster Products, LLC

FDA Regulatory Profile

Schuster Products, LLC has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 17, 2026 · VAI

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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
Inspections3Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 17, 2026Hales Corners, WIFood/CosmeticsVoluntary Action Indicated (VAI)3007090289
Jul 13, 2016Sturtevant, WIFood/CosmeticsNo Action Indicated (NAI)3009915330
Apr 19, 2012Hales Corners, WIFood/CosmeticsNo Action Indicated (NAI)3007090289

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 3007090289Hales Corners, WI2Apr 17, 2026
FEI 3009915330Sturtevant, WI1Jul 13, 2016

FDA data resources

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