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Compass International Innovations Inc.

FDA Regulatory Profile

Compass International Innovations Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jul 10, 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 10, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 10, 2025Rochester, MNDevicesNo Action Indicated (NAI)2183671
Jun 21, 2023Rochester, MNDevicesNo Action Indicated (NAI)2183671
Sep 17, 2018Rochester, MNDevicesNo Action Indicated (NAI)2183671
Nov 15, 2011Rochester, MNDevicesNo Action Indicated (NAI)2183671

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 2183671Rochester, MN4Jul 10, 2025

FDA data resources

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