SupplierRadar

Torres y Ribelles, S.A.

FDA import alert and refusal historyDos Hermanas, SpainFEI 3004250531

Recorded by FDA as TORRES Y RIBELLES, S.A.

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Example subjectTorres y Ribelles, S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Torres y Ribelles, S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on November 15, 2017, 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 Torres y Ribelles, S.A.

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

2017

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2012

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

Questions about Torres y Ribelles, S.A.

Is Torres y Ribelles, S.A. on an FDA import alert?
No listing for Torres y Ribelles, 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 Torres y Ribelles, S.A.?
No FDA import refusals for Torres y Ribelles, S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Torres y Ribelles, S.A. last inspected by FDA?
FDA's most recent inspection of Torres y Ribelles, S.A. with a final classification is dated November 15, 2017 and was classified NAI (No Action Indicated).
What is Torres y Ribelles, S.A.'s FEI number?
Torres y Ribelles, S.A.'s FDA Establishment Identifier (FEI) is 3004250531.

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Example subjectTorres y Ribelles, 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.