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Nimbic Systems, Inc.

FDA Regulatory Profile

Nimbic Systems, Inc. has 0 FDA recalls, 1 inspection, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jan 6, 2017 · VAI
Latest 510(k)
Dec 20, 2013

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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
Inspections1Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 6, 2017Stafford, TXDevicesVoluntary Action Indicated (VAI)3006412720

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
K123006AIR BARRIER SYSTEM (ABS)Dec 20, 2013
K092801ABS BLOWER, ABS NOZZLE, MODEL 1001May 20, 2011

FDA data resources