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Roni Ferreira de Freitas

FDA import alert and refusal historyRio De Janeiro, BrazilFEI 3032202045

Recorded by FDA as RONI FERREIRA DE FREITAS

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Example subjectRoni Ferreira de Freita added to Import Alert 16-129 (red list)

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As of October 26, 2026, Roni Ferreira de Freitas is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 5, 2026, most often for salmonella (SALMONELLA).

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

Current status

Import alerts
Not listed
Last import refusal
Pepper, black, ground, cracked (spice) · SALMONELLA
Last warning letter
None found
Last inspection
None on record

Every FDA record for Roni Ferreira de Freitas

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

2026

  1. Import refusal
    Refused, Pepper, black, ground, cracked (spice)SALMONELLAEntry J37-0013798-0
    Source

Refusal charges, in plain English

  • SALMONELLA1 refused line

    Salmonella

    The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Roni Ferreira de Freitas

Is Roni Ferreira de Freitas on an FDA import alert?
No listing for Roni Ferreira de Freitas 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 Roni Ferreira de Freitas?
Yes. FDA refused 1 shipment line from Roni Ferreira de Freitas on May 5, 2026. The most recent, on May 5, 2026, was pepper, black, ground, cracked (spice), charged as SALMONELLA (salmonella).
Why did FDA refuse Roni Ferreira de Freitas's shipments?
The most frequent charge is SALMONELLA (salmonella, 1 line).
What is Roni Ferreira de Freitas's FEI number?
Roni Ferreira de Freitas's FDA Establishment Identifier (FEI) is 3032202045.

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Example subjectRoni Ferreira de Freita 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.