Vonco Products

FDA Regulatory Profile

Vonco Products has 0 FDA recalls, 3 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 10, 2025 · VAI
Latest 510(k)
Jul 10, 2023

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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) clearances2Oct 4, 2026Not statedCurrent
Inspections3Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 10, 2025Trevor, WIDevicesVoluntary Action Indicated (VAI)1419562
Aug 30, 2024Fortville, INDevicesNo Action Indicated (NAI)1000139922
Jun 29, 2017Trevor, WIDevicesNo Action Indicated (NAI)1419562

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
K223683EnteraLoc FlowJul 10, 2023
K210971EnteraLoc FlowAug 18, 2021