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Micron Corp.

FDA Regulatory Profile

Micron Corp. has 0 FDA recalls, 4 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest inspection
Dec 19, 2025 · VAI
Latest 510(k)
Mar 8, 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) clearances5Oct 4, 2026Not statedCurrent
Inspections4Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 19, 2025Wilmington, DEDrugsVoluntary Action Indicated (VAI)1000522074
Nov 5, 2021Wilmington, DEDrugsVoluntary Action Indicated (VAI)1000522074
Aug 10, 2015Wilmington, DEDrugsNo Action Indicated (NAI)1000522074
Apr 26, 2011Wilmington, DEDrugsNo Action Indicated (NAI)1000522074

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
K171150AW-100Mar 8, 2018
K161639Y-MICDec 22, 2016
K133170QUICK JET MMar 28, 2014
K032995SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL)Nov 20, 2003
K991239VIP 60 (2H), MODEL 115-000-1, VIP 60 (4H), MODEL 115-000-2Oct 18, 1999

FDA data resources