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Esperanza del Castillo, S. L.

FDA import alert and refusal historyPulgar, SpainFEI 3004690553

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Example subjectEsperanza del Castillo, S. L added to Import Alert 16-129 (red list)

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As of October 26, 2026, Esperanza del Castillo, S. L. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 17, 2020, 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 Esperanza del Castillo, S. L.

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

2020

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

2011

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

Questions about Esperanza del Castillo, S. L.

Is Esperanza del Castillo, S. L. on an FDA import alert?
No listing for Esperanza del Castillo, S. L. 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 Esperanza del Castillo, S. L.?
No FDA import refusals for Esperanza del Castillo, S. L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Esperanza del Castillo, S. L. last inspected by FDA?
FDA's most recent inspection of Esperanza del Castillo, S. L. with a final classification is dated January 17, 2020 and was classified VAI (Voluntary Action Indicated).
What is Esperanza del Castillo, S. L.'s FEI number?
Esperanza del Castillo, S. L.'s FDA Establishment Identifier (FEI) is 3004690553.

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Example subjectEsperanza del Castillo, S. L 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.