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Rostein, Daniel MD SC

FDA Regulatory Profile

Rostein, Daniel MD SC has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 14, 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 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 14, 2025Oak Brook, ILBiologicsNo Action Indicated (NAI)3009840486
Sep 11, 2023Oak Brook, ILBiologicsNo Action Indicated (NAI)3009840486
Jul 19, 2018Oak Brook, ILBiologicsNo Action Indicated (NAI)3009840486
Apr 19, 2016Oak Brook, ILBiologicsNo Action Indicated (NAI)3009840486
Jun 30, 2014Oak Brook, ILBiologicsNo Action Indicated (NAI)3009840486

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 3009840486Oak Brook, IL5Jul 14, 2025

FDA data resources

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