Aman Kapoor Inc

FDA Regulatory Profile

Aman Kapoor Inc has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Mar 2, 2026 · 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
Inspections5Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 2, 2026Elk Grove Village, ILFood/CosmeticsVoluntary Action Indicated (VAI)3007871402
Aug 24, 2023Elk Grove Village, ILFood/CosmeticsOfficial Action Indicated (OAI)3007871402
Dec 29, 2021Elk Grove Village, ILFood/CosmeticsVoluntary Action Indicated (VAI)3007871402
Dec 17, 2020Elk Grove Village, ILFood/CosmeticsOfficial Action Indicated (OAI)3007871402
Sep 13, 2017Elk Grove Village, ILFood/CosmeticsVoluntary Action Indicated (VAI)3007871402

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 3007871402Elk Grove Village, IL5Mar 2, 2026

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