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Evonik Corporation

FDA Regulatory Profile

Evonik Corporation has 0 FDA recalls, 20 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 11, 2026 · 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
Inspections20Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 11, 2026Theodore, ALFood/CosmeticsNo Action Indicated (NAI)3007772046
Sep 11, 2025Lafayette, INDrugsNo Action Indicated (NAI)1813682
May 22, 2025Etowah, TNFood/CosmeticsNo Action Indicated (NAI)1023148
Dec 10, 2024Birmingham, ALDrugsVoluntary Action Indicated (VAI)3012757951
Oct 22, 2024Chester, PAFood/CosmeticsNo Action Indicated (NAI)3004334887
Dec 11, 2023Theodore, ALFood/CosmeticsNo Action Indicated (NAI)3007772046
Oct 11, 2023Mapleton, ILFood/CosmeticsNo Action Indicated (NAI)1419649
Jan 16, 2020Lafayette, INVeterinaryNo Action Indicated (NAI)1813682
Aug 10, 2018Birmingham, ALDrugsVoluntary Action Indicated (VAI)3012757951
May 24, 2018Mapleton, ILFood/CosmeticsNo Action Indicated (NAI)1419649
Jan 12, 2018Lafayette, INVeterinaryNo Action Indicated (NAI)1813682
Feb 2, 2017Chester, PAFood/CosmeticsNo Action Indicated (NAI)3004334887
Apr 12, 2016Etowah, TNFood/CosmeticsNo Action Indicated (NAI)1023148
Aug 4, 2015Lafayette, INDrugsNo Action Indicated (NAI)1813682
Sep 16, 2014Lafayette, INVeterinaryNo Action Indicated (NAI)1813682
Jun 17, 2014Mapleton, ILFood/CosmeticsNo Action Indicated (NAI)1419649
May 23, 2012Chester, PAFood/CosmeticsNo Action Indicated (NAI)3004334887
Mar 23, 2012Lafayette, INDrugsNo Action Indicated (NAI)1813682
Mar 13, 2012Mapleton, ILDrugsNo Action Indicated (NAI)1419649
Mar 12, 2010Lafayette, INDrugsNo Action Indicated (NAI)1813682

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 3007772046Theodore, AL2Aug 11, 2026
FEI 1813682Lafayette, IN7Sep 11, 2025
FEI 1023148Etowah, TN2May 22, 2025
FEI 3012757951Birmingham, AL2Dec 10, 2024
FEI 3004334887Chester, PA3Oct 22, 2024
FEI 1419649Mapleton, IL4Oct 11, 2023

FDA data resources

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