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Borde SA

FDA import alert and refusal historySaugues, FranceFEI 3002809317

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

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As of October 25, 2026, Borde SA is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between May 19, 2017 and January 21, 2026, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Mushrooms and other fungi products, whole (button), n.e.c. · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Borde SA

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

2026

  1. Import refusal
    Refused, Mushrooms and other fungi products, whole (button), n.e.c.FILTHYEntry 506-7541020-8
    Source

2023

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

2017

  1. Import refusal
    Refused, Mushrooms and other fungi products, pieces and stems, sliced, n.e.c.FILTHYEntry 734-0074126-7
    Source

2011

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

Refusal charges, in plain English

  • FILTHY2 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Borde SA

Is Borde SA on an FDA import alert?
No listing for Borde SA appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the France page.
Has FDA refused shipments from Borde SA?
Yes. FDA refused 2 shipment lines from Borde SA between May 19, 2017 and January 21, 2026. The most recent, on January 21, 2026, was mushrooms and other fungi products, whole (button), n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Borde SA's shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
When was Borde SA last inspected by FDA?
FDA's most recent inspection of Borde SA with a final classification is dated September 19, 2023 and was classified VAI (Voluntary Action Indicated).
What is Borde SA's FEI number?
Borde SA's FDA Establishment Identifier (FEI) is 3002809317.

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Example subjectBorde 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.