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Sunrise Distributors Inc

FDA Regulatory Profile

Sunrise Distributors Inc has 0 FDA recalls, 3 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Apr 15, 2021 · OAI

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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
Inspections3Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 15, 2021Elk Grove Village, ILFood/CosmeticsOfficial Action Indicated (OAI)3009214777
Dec 5, 2019Elk Grove Village, ILFood/CosmeticsOfficial Action Indicated (OAI)3009214777
Jul 9, 2018Elk Grove Village, ILFood/CosmeticsVoluntary Action Indicated (VAI)3009214777

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 3009214777Elk Grove Village, IL3Apr 15, 2021

FDA data resources

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