Corim International Coffee Inc.

FDA Regulatory Profile

Corim International Coffee Inc. has 4 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
F-0387-2023 · Class III · Jan 13, 2023
Latest inspection
May 22, 2025 · NAI

Reviewing Corim International Coffee Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Corim International Coffee Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls4Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections4Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
F-0387-2023Class IIICocoa de Aroma, 24 ct single serve coffee pods assorted (12.7 oz carton containing Peanut Butter…Jan 13, 2023
F-0389-2023Class IIIJersey Charm, 24 ct single serve coffee pods (12.7 oz. carton)Jan 13, 2023
F-0390-2023Class IIIColonial Coffee, 12 ct single serve coffee pods (4.44 oz. carton)Jan 13, 2023
F-0388-2023Class IIISmart Sips, 24 ct single serve coffee pods (12.7 oz carton)Jan 13, 2023

Recent FDA Inspections

DateSiteProductClassificationFEI
May 22, 2025Brick, NJFood/CosmeticsNo Action Indicated (NAI)3004319616
May 22, 2025Brick, NJFood/CosmeticsNo Action Indicated (NAI)3012184120
Aug 3, 2023Brick, NJFood/CosmeticsNo Action Indicated (NAI)3004319616
Feb 9, 2012Brick, NJFood/CosmeticsVoluntary Action Indicated (VAI)3004319616

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 3004319616Brick, NJ3May 22, 2025
FEI 3012184120Brick, NJ1May 22, 2025

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