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Resilience US, LLC

FDA Regulatory Profile

Resilience US, LLC has 0 FDA recalls, 21 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Jan 21, 2025 · VAI

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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
Inspections21Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 21, 2025West Chester, OHDrugsVoluntary Action Indicated (VAI)3006316363
Aug 21, 2019Allston, MADrugsNo Action Indicated (NAI)1000305672
Aug 9, 2019West Chester, OHDevicesNo Action Indicated (NAI)3006316363
Mar 8, 2018West Chester, OHDrugsVoluntary Action Indicated (VAI)3006316363
Sep 14, 2017Allston, MADrugsNo Action Indicated (NAI)1000305672
Sep 7, 2017West Chester, OHDrugsNo Action Indicated (NAI)3006316363
Aug 11, 2017Allston, MADrugsVoluntary Action Indicated (VAI)1000305672
Jun 27, 2017West Chester, OHDrugsNo Action Indicated (NAI)3006316363
Aug 24, 2016West Chester, OHDrugsNo Action Indicated (NAI)3006316363
Nov 3, 2015West Chester, OHDrugsNo Action Indicated (NAI)3006316363
Jul 28, 2015West Chester, OHDrugsNo Action Indicated (NAI)3006316363
Sep 25, 2014Allston, MADrugsVoluntary Action Indicated (VAI)1000305672
Jul 22, 2014West Chester, OHDrugsVoluntary Action Indicated (VAI)3006316363
Apr 9, 2013West Chester, OHDrugsNo Action Indicated (NAI)3006316363
Jul 11, 2012West Chester, OHDrugsVoluntary Action Indicated (VAI)3006316363
Oct 15, 2010West Chester, OHDrugsNo Action Indicated (NAI)3006316363
Jan 29, 2010West Chester, OHDrugsNo Action Indicated (NAI)3006316363
Dec 23, 2009West Chester, OHDrugsOfficial Action Indicated (OAI)3006316363
Nov 13, 2009Allston, MADrugsOfficial Action Indicated (OAI)1000305672
May 28, 2009Allston, MADrugsOfficial Action Indicated (OAI)1000305672

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 3006316363West Chester, OH14Jan 21, 2025
FEI 1000305672Allston, MA7Aug 21, 2019

FDA data resources

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