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Perma Pure, LLC

FDA Regulatory Profile

Perma Pure, LLC has 0 FDA recalls, 7 inspections, 1 510(k) clearance and 1 compliance action on record.

Latest inspection
Mar 6, 2026 · NAI
Latest 510(k)
Nov 12, 2020

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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) clearances1Oct 4, 2026Not statedCurrent
Inspections7Oct 25, 2026Not statedCurrent
Compliance actions1Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 6, 2026Lakewood, NJDevicesNo Action Indicated (NAI)2244684
Jan 3, 2020Lakewood, NJDevicesNo Action Indicated (NAI)2244684
Jan 21, 2016Lakewood, NJDevicesNo Action Indicated (NAI)2244684
Jul 9, 2013Lakewood, NJDevicesVoluntary Action Indicated (VAI)2244684
Sep 19, 2011Lakewood, NJDevicesNo Action Indicated (NAI)2244684
Mar 18, 2011Lakewood, NJDevicesOfficial Action Indicated (OAI)2244684
Aug 23, 2010Lakewood, NJDevicesOfficial Action Indicated (OAI)2244684

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
K193411O2asis Personal Oxygen HumidifierNov 12, 2020

FDA data resources