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Usina Sao Francisco S.A.

FDA import alert and refusal historySertaozinho, BrazilFEI 3010121283

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Example subjectUsina Sao Francisco S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Usina Sao Francisco S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on August 28, 2019, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)

Every FDA record for Usina Sao Francisco S.A.

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

2019

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

2015

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

Questions about Usina Sao Francisco S.A.

Is Usina Sao Francisco S.A. on an FDA import alert?
No listing for Usina Sao Francisco S.A. 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 Usina Sao Francisco S.A.?
No FDA import refusals for Usina Sao Francisco S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Usina Sao Francisco S.A. last inspected by FDA?
FDA's most recent inspection of Usina Sao Francisco S.A. with a final classification is dated August 28, 2019 and was classified VAI (Voluntary Action Indicated).
What is Usina Sao Francisco S.A.'s FEI number?
Usina Sao Francisco S.A.'s FDA Establishment Identifier (FEI) is 3010121283.

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Example subjectUsina Sao Francisco 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.