Colcafe S.A.
FDA import alert and refusal historyMedellin, ColombiaFEI 3005809346
As of October 25, 2026, Colcafe S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on August 1, 2018, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Coffee, ground · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Colcafe S.A.
4 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 4 lines in one entry: Coffee, groundNO ENGLISHEntry AMN-0040672-4Show 4 linesHide lines
- Refused, Coffee, groundNO ENGLISHEntry AMN-0040672-4Source
- Refused, Coffee, groundNO ENGLISHEntry AMN-0040672-4Source
- Refused, Coffee, groundNO ENGLISHEntry AMN-0040672-4Source
- Refused, Coffee, groundNO ENGLISHEntry AMN-0040672-4Source
Refusal charges, in plain English
- NO ENGLISH4 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Colcafe S.A.
- Is Colcafe S.A. on an FDA import alert?
- No listing for Colcafe S.A. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
- Has FDA refused shipments from Colcafe S.A.?
- Yes. FDA refused 4 shipment lines from Colcafe S.A. on August 1, 2018. The most recent, on August 1, 2018, was coffee, ground, charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Colcafe S.A.'s shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 4 lines).
- What is Colcafe S.A.'s FEI number?
- Colcafe S.A.'s FDA Establishment Identifier (FEI) is 3005809346.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.