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Livent USA Corp

FDA Regulatory Profile

Livent USA Corp has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 11, 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
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 11, 2025Bessemer City, NCDrugsNo Action Indicated (NAI)1015213
Feb 7, 2020Bessemer City, NCDrugsVoluntary Action Indicated (VAI)1015213
Feb 16, 2018Bessemer City, NCDrugsVoluntary Action Indicated (VAI)1015213
Sep 27, 2016Bessemer City, NCDrugsNo Action Indicated (NAI)1015213
May 2, 2013Bessemer City, NCDrugsNo Action Indicated (NAI)1015213
Apr 20, 2010Bessemer City, NCDrugsNo Action Indicated (NAI)1015213

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 1015213Bessemer City, NC6Sep 11, 2025

FDA data resources

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