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Benchmark Electronics, Inc.

FDA Regulatory Profile

Benchmark Electronics, Inc. has 0 FDA recalls, 13 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jun 4, 2026 · 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
Inspections13Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 4, 2026Rochester, MNDevicesNo Action Indicated (NAI)3000204692
Apr 18, 2025Nashua, NHDevicesNo Action Indicated (NAI)3008986341
Jun 17, 2021Winona, MNDevicesNo Action Indicated (NAI)3000203466
Aug 26, 2020Nashua, NHDevicesVoluntary Action Indicated (VAI)3008986341
May 2, 2019Rochester, MNDevicesNo Action Indicated (NAI)3000204692
Jul 24, 2018San Jose, CABiologicsNo Action Indicated (NAI)3010510475
Apr 25, 2018Winona, MNDevicesNo Action Indicated (NAI)3000203466
Apr 8, 2014Winona, MNDevicesNo Action Indicated (NAI)3000203466
Dec 14, 2011Winona, MNDevicesNo Action Indicated (NAI)3000203466
Nov 17, 2011Rochester, MNDevicesNo Action Indicated (NAI)3000204692
May 19, 2011Winona, MNDevicesNo Action Indicated (NAI)3000203466
Dec 17, 2009Winona, MNDevicesNo Action Indicated (NAI)3000203466
May 14, 2009Rochester, MNDevicesNo Action Indicated (NAI)3000204692

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 3000204692Rochester, MN4Jun 4, 2026
FEI 3008986341Nashua, NH2Apr 18, 2025
FEI 3000203466Winona, MN6Jun 17, 2021
FEI 3010510475San Jose, CA1Jul 24, 2018

FDA data resources

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