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Postabon S.A.

FDA import alert and refusal historyMedellin, ColombiaFEI 3004118430

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Example subjectPostabon S.A added to Import Alert 16-129 (red list)

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As of October 25, 2026, Postabon S.A. (Medellin, Colombia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for apple flavored carbonatred soft drink; apple flavored carbonated soft drink, published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Postabon S.A.

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listapple flavored carbonatred soft drink; apple flavored carbonated soft drink
    Source

Questions about Postabon S.A.

Is Postabon S.A. on an FDA import alert?
Yes. As of October 25, 2026, Postabon S.A. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for apple flavored carbonatred soft drink; apple flavored carbonated soft drink; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Postabon S.A.?
No FDA import refusals for Postabon S.A. appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Postabon S.A.'s FEI number?
Postabon S.A.'s FDA Establishment Identifier (FEI) is 3004118430.
Can shipments from Postabon S.A. still enter the U.S.?
Shipments of apple flavored carbonatred soft drink; apple flavored carbonated soft drink from Postabon S.A. can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectPostabon S.A added to Import Alert 16-129 (red list)

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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.