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Rms Company

FDA Regulatory Profile

Rms Company has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 12, 2025 · 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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 12, 2025Minneapolis, MNDevicesVoluntary Action Indicated (VAI)1000116116
May 18, 2022Minneapolis, MNDevicesVoluntary Action Indicated (VAI)1000116116
Jan 6, 2016Minneapolis, MNDevicesNo Action Indicated (NAI)1000116116
Jun 20, 2012Minneapolis, MNDevicesNo Action Indicated (NAI)1000116116
Feb 27, 2009Minneapolis, MNDevicesNo Action Indicated (NAI)1000116116

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 1000116116Minneapolis, MN5Sep 12, 2025

FDA data resources

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