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Bresson S.A

FDA import alert and refusal historyGuayaquil, EcuadorFEI 3004350475

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

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As of October 25, 2026, Bresson S.A has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on November 20, 2019, was classified NAI (No Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Bresson S.A

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

2019

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

2015

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2014

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2010

  1. Inspection
    Inspection classified OAI (Official Action Indicated)Foodborne Biological Hazards
    Source

Questions about Bresson S.A

Is Bresson S.A on an FDA import alert?
No listing for Bresson 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 Ecuador page.
Has FDA refused shipments from Bresson S.A?
No FDA import refusals for Bresson S.A appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Bresson S.A last inspected by FDA?
FDA's most recent inspection of Bresson S.A with a final classification is dated November 20, 2019 and was classified NAI (No Action Indicated).
What is Bresson S.A's FEI number?
Bresson S.A's FDA Establishment Identifier (FEI) is 3004350475.

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Example subjectBresson S. 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.