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Albemarle US, Inc.

FDA Regulatory Profile

Albemarle US, Inc. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 8, 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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 8, 2025Kings Mountain, NCDrugsNo Action Indicated (NAI)1032207
Jan 25, 2019Kings Mountain, NCDrugsNo Action Indicated (NAI)1032207
Mar 12, 2015Kings Mountain, NCDrugsNo Action Indicated (NAI)1032207
May 19, 2011Kings Mountain, NCDrugsNo Action Indicated (NAI)1032207
Mar 31, 2009Kings Mountain, NCDrugsNo Action Indicated (NAI)1032207

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 1032207Kings Mountain, NC5Sep 8, 2025

FDA data resources

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