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Urgel Ganadera S.A.

FDA import alert and refusal historyJuneda, SpainFEI 3010115706

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Example subjectUrgel Ganadera S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Urgel Ganadera S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between July 11, 2017 and June 30, 2020, most often for salmonella (SALMONELLA).

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

Current status

Import alerts
Not listed
Last import refusal
Quail · SALMONELLA
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Urgel Ganadera S.A.

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

2020

  1. Import refusal
    Refused, QuailSALMONELLAEntry DP4-8345968-2
    Source
  2. Import refusal
    Refused, QuailSALMONELLAEntry DP4-8341160-0
    Source

2019

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

2017

  1. Import refusal
    Refused, QuailSALMONELLAEntry DP4-8136025-4
    Source

Refusal charges, in plain English

  • SALMONELLA3 refused lines

    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 Urgel Ganadera S.A.

Is Urgel Ganadera S.A. on an FDA import alert?
No listing for Urgel Ganadera 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 Spain page.
Has FDA refused shipments from Urgel Ganadera S.A.?
Yes. FDA refused 3 shipment lines from Urgel Ganadera S.A. between July 11, 2017 and June 30, 2020. The most recent, on June 30, 2020, was quail, charged as SALMONELLA (salmonella).
Why did FDA refuse Urgel Ganadera S.A.'s shipments?
The most frequent charge is SALMONELLA (salmonella, 3 lines).
When was Urgel Ganadera S.A. last inspected by FDA?
FDA's most recent inspection of Urgel Ganadera S.A. with a final classification is dated September 10, 2019 and was classified VAI (Voluntary Action Indicated).
What is Urgel Ganadera S.A.'s FEI number?
Urgel Ganadera S.A.'s FDA Establishment Identifier (FEI) is 3010115706.

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Example subjectUrgel Ganadera 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.