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RFI, LLC.

FDA Regulatory Profile

RFI, LLC. has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 22, 2026 · NAI

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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
Inspections5Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 22, 2026Orangeburg, NYFood/CosmeticsNo Action Indicated (NAI)3020270675
Jun 10, 2025Broomfield, COFood/CosmeticsVoluntary Action Indicated (VAI)3004693308
Jan 28, 2020Broomfield, COFood/CosmeticsVoluntary Action Indicated (VAI)3004693308
Sep 20, 2017Broomfield, COFood/CosmeticsNo Action Indicated (NAI)3004693308
Mar 16, 2012Broomfield, COFood/CosmeticsNo Action Indicated (NAI)3004693308

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 3020270675Orangeburg, NY1Apr 22, 2026
FEI 3004693308Broomfield, CO4Jun 10, 2025

FDA data resources

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