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Sarl Fromagerie Poerucci

FDA import alert and refusal historyVescovato, FranceFEI 3005687950

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Example subjectSarl Fromagerie Poerucc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sarl Fromagerie Poerucci is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on June 14, 2017, most often for listeria monocytogenes (LISTERIA).

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

Current status

Import alerts
Not listed
Last import refusal
Cheese, sheep, n.e.c. · LISTERIA
Last warning letter
None found
Last inspection
None on record

Every FDA record for Sarl Fromagerie Poerucci

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

2017

  1. Import refusal
    Refused, 2 lines in one entry: Cheese, sheep, n.e.c.LISTERIAEntry DP4-8129180-6Show 2 lines
    Source

Refusal charges, in plain English

  • LISTERIA2 refused lines

    Listeria monocytogenes

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

Questions about Sarl Fromagerie Poerucci

Is Sarl Fromagerie Poerucci on an FDA import alert?
No listing for Sarl Fromagerie Poerucci appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.
Has FDA refused shipments from Sarl Fromagerie Poerucci?
Yes. FDA refused 2 shipment lines from Sarl Fromagerie Poerucci on June 14, 2017. The most recent, on June 14, 2017, was cheese, sheep, n.e.c., charged as LISTERIA (listeria monocytogenes).
Why did FDA refuse Sarl Fromagerie Poerucci's shipments?
The most frequent charge is LISTERIA (listeria monocytogenes, 2 lines).
What is Sarl Fromagerie Poerucci's FEI number?
Sarl Fromagerie Poerucci's FDA Establishment Identifier (FEI) is 3005687950.

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Example subjectSarl Fromagerie Poerucc 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.