Hanuri Distribution, Inc.

FDA Regulatory Profile

Hanuri Distribution, Inc. has 0 FDA recalls, 4 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Mar 26, 2026 · VAI
Latest 510(k)
Oct 21, 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) clearances2Oct 4, 2026Not statedCurrent
Inspections4Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 26, 2026Chatsworth, CADevicesVoluntary Action Indicated (VAI)3007778244
Jul 22, 2021Chatsworth, CADevicesNo Action Indicated (NAI)3007778244
Nov 9, 2016Chatsworth, CADevicesVoluntary Action Indicated (VAI)3007778244
Dec 9, 2013Chatsworth, CADevicesVoluntary Action Indicated (VAI)3007778244

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
K202044Powerpress Recovery UnitOct 21, 2020
K110276POWERPRESS UNITNov 9, 2011