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Nextern Innovation, LLC.

FDA Regulatory Profile

Nextern Innovation, LLC. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Nov 4, 2025 · 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
Inspections4Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 4, 2025Maple Grove, MNDevicesNo Action Indicated (NAI)3031976597
Nov 8, 2021Maple Grove, MNDevicesNo Action Indicated (NAI)3031976597
Jul 25, 2017Maple Grove, MNDevicesNo Action Indicated (NAI)3031976597
Feb 23, 2012Maple Grove, MNDevicesNo Action Indicated (NAI)3031976597

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 3031976597Maple Grove, MN4Nov 4, 2025

FDA data resources

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