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Matriz Do Acai Comercio Exportac

FDA import alert and refusal historySao Paulo, BrazilFEI 3009605841

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Example subjectMatriz Do Acai Comercio Exporta added to Import Alert 16-129 (red list)

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As of October 26, 2026, Matriz Do Acai Comercio Exportac (Sao Paulo, Brazil) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for acai juice, published by FDA on December 13, 2012, 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 Matriz Do Acai Comercio Exportac

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

2012

  1. Import alert listing
    Listed on Import Alert 45-02red listAcai Juice
    Source

Questions about Matriz Do Acai Comercio Exportac

Is Matriz Do Acai Comercio Exportac on an FDA import alert?
Yes. As of October 26, 2026, Matriz Do Acai Comercio Exportac is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for acai juice; FDA published the listing on December 13, 2012.
Has FDA refused shipments from Matriz Do Acai Comercio Exportac?
No FDA import refusals for Matriz Do Acai Comercio Exportac appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Matriz Do Acai Comercio Exportac's FEI number?
Matriz Do Acai Comercio Exportac's FDA Establishment Identifier (FEI) is 3009605841.
Can shipments from Matriz Do Acai Comercio Exportac still enter the U.S.?
Shipments of acai juice from Matriz Do Acai Comercio Exportac 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 subjectMatriz Do Acai Comercio Exporta 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.