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Avent, Inc.

FDA Regulatory Profile

Avent, Inc. has 0 FDA recalls, 12 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 10, 2025 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections12Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 10, 2025Tucson, AZDrugsNo Action Indicated (NAI)3006646024
Feb 21, 2020Tucson, AZDrugsVoluntary Action Indicated (VAI)3006646024
Apr 5, 2018Fort Lauderdale, FLDevicesNo Action Indicated (NAI)3014274845
Nov 28, 2016Tucson, AZDevicesNo Action Indicated (NAI)3006646024
Apr 2, 2015Concord, CADevicesNo Action Indicated (NAI)3009761594
Nov 5, 2014Tucson, AZDrugsNo Action Indicated (NAI)3006646024
May 3, 2013Tucson, AZDevicesNo Action Indicated (NAI)3006646024
Aug 23, 2012Concord, CADevicesNo Action Indicated (NAI)3009761594
Oct 28, 2011Tucson, AZDevicesVoluntary Action Indicated (VAI)3006646024
Mar 31, 2010Tucson, AZDevicesNo Action Indicated (NAI)3006646024
Dec 2, 2009Tucson, AZDrugsNo Action Indicated (NAI)3006646024
Feb 4, 2009Tucson, AZDevicesNo Action Indicated (NAI)3006646024

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3006646024Tucson, AZ9Jul 10, 2025
FEI 3014274845Fort Lauderdale, FL1Apr 5, 2018
FEI 3009761594Concord, CA2Apr 2, 2015

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.