BASF SE

FDA Regulatory Profile

BASF SE has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 29, 2024 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections6Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 29, 2024Ludwigshafen Am Rhein, GermanyDrugsVoluntary Action Indicated (VAI)3002903906
Sep 16, 2020Ludwigshafen Am Rhein, GermanyDrugsVoluntary Action Indicated (VAI)3002903906
Jul 13, 2018Ludwigshafen Am Rhein, GermanyDrugsVoluntary Action Indicated (VAI)3002903906
Mar 10, 2016Ludwigshafen Am Rhein, GermanyDrugsNo Action Indicated (NAI)3002903906
Jun 27, 2013Ludwigshafen Am Rhein, GermanyDrugsNo Action Indicated (NAI)3002903906
Mar 17, 2010Ludwigshafen Am Rhein, GermanyDrugsVoluntary Action Indicated (VAI)3002903906

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 3002903906Ludwigshafen Am Rhein, Germany6Aug 29, 2024

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