CNMC Company, Inc.

FDA Regulatory Profile

CNMC Company, Inc. has 0 FDA recalls, 5 inspections, 2 510(k) clearances and 1 compliance action on record.

Latest inspection
Feb 12, 2026 · NAI
Latest 510(k)
Aug 7, 2018

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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
Inspections5Oct 25, 2026Not statedCurrent
Compliance actions1Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 12, 2026Nashville, TNDevicesNo Action Indicated (NAI)3006073271
Sep 14, 2023Nashville, TNDevicesNo Action Indicated (NAI)3006073271
Mar 9, 2018Nashville, TNDevicesVoluntary Action Indicated (VAI)3006073271
Jul 8, 2015Nashville, TNDevicesVoluntary Action Indicated (VAI)3006073271
Feb 4, 2014Nashville, TNDevicesNo Action Indicated (NAI)3006073271

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
K173848Model WP-3840 and WP-3040Aug 7, 2018
K150265Model 206 Electrometer/DosimeterSep 3, 2015