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Congelados Del Monte, S.A.

FDA import alert and refusal historyBarrel De Heredia, Costa RicaFEI 3004380624

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Example subjectCongelados Del Monte, S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Congelados Del Monte, S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on July 20, 2017, 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 Congelados Del Monte, S.A.

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

2017

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

2015

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

Questions about Congelados Del Monte, S.A.

Is Congelados Del Monte, S.A. on an FDA import alert?
No listing for Congelados Del Monte, 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 Costa Rica page.
Has FDA refused shipments from Congelados Del Monte, S.A.?
No FDA import refusals for Congelados Del Monte, S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Congelados Del Monte, S.A. last inspected by FDA?
FDA's most recent inspection of Congelados Del Monte, S.A. with a final classification is dated July 20, 2017 and was classified VAI (Voluntary Action Indicated).
What is Congelados Del Monte, S.A.'s FEI number?
Congelados Del Monte, S.A.'s FDA Establishment Identifier (FEI) is 3004380624.

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Example subjectCongelados Del Monte, 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.