SupplierRadar

Empresa Brasileira de Bebidas e Alimentos SA

FDA import alert and refusal historyAracati, BrazilFEI 3004024988

Recorded by FDA as EMPRESA BRASILEIRA DE BEBIDAS E ALIMENTOS SA

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Example subjectEmpresa Brasileira de Bebidas e Alimentos S added to Import Alert 16-129 (red list)

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As of October 26, 2026, Empresa Brasileira de Bebidas e Alimentos SA is not on any FDA import alert in SupplierRadar's records; FDA refused 5 of its shipment lines between August 11, 2025 and November 2, 2025, most often for no scheduled process filed (NO PROCESS).

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

Current status

Import alerts
Not listed
Last import refusal
Subtropical/tropical, mixed, juices or concentrates · NO PROCESS
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Empresa Brasileira de Bebidas e Alimentos SA

6 records, newest first. Each line links to the FDA page it came from.

2025

  1. Import refusal
    Refused, 4 lines in one entry: Subtropical/tropical, mixed, juices or concentratesNO PROCESSEntry AVV-9975071-7Show 4 lines
    • Refused, Subtropical/tropical, mixed, juices or concentratesNO PROCESSEntry AVV-9975071-7Source
    • Refused, Subtropical/tropical, mixed, juices or concentratesNO PROCESSEntry AVV-9975071-7Source
    • Refused, Subtropical/tropical, mixed, juices or concentratesNO PROCESSEntry AVV-9975071-7Source
    • Refused, Subtropical/tropical, mixed, juices or concentratesNO PROCESSEntry AVV-9975071-7Source
    Source
  2. Import refusal
    Refused, Cashew fruit, subtropical and tropical fruit, juices, milk, creme, drinks and nectarsLACKS N/CNO ENGLISHNUTRIT LBLNO PROCESSEntry K51-0108300-1
    Source

2014

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • NO PROCESS5 refused lines

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • NO ENGLISH1 refused line

    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.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Empresa Brasileira de Bebidas e Alimentos SA

Is Empresa Brasileira de Bebidas e Alimentos SA on an FDA import alert?
No listing for Empresa Brasileira de Bebidas e Alimentos SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Brazil page.
Has FDA refused shipments from Empresa Brasileira de Bebidas e Alimentos SA?
Yes. FDA refused 5 shipment lines from Empresa Brasileira de Bebidas e Alimentos SA between August 11, 2025 and November 2, 2025. The most recent, on November 2, 2025, was subtropical/tropical, mixed, juices or concentrates, charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Empresa Brasileira de Bebidas e Alimentos SA's shipments?
The most frequent charges are NO PROCESS (no scheduled process filed, 5 lines) and LACKS N/C (net quantity statement missing, 1 line).
When was Empresa Brasileira de Bebidas e Alimentos SA last inspected by FDA?
FDA's most recent inspection of Empresa Brasileira de Bebidas e Alimentos SA with a final classification is dated September 23, 2014 and was classified NAI (No Action Indicated).
What is Empresa Brasileira de Bebidas e Alimentos SA's FEI number?
Empresa Brasileira de Bebidas e Alimentos SA's FDA Establishment Identifier (FEI) is 3004024988.

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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.