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Productos Marinos Del Norte

FDA import alert and refusal historyCaldera, ChileFEI 1000208181

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Example subjectProductos Marinos Del Nort added to Import Alert 16-129 (red list)

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As of October 26, 2026, Productos Marinos Del Norte (Caldera, Chile) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for fresh and frozen, published by FDA on September 10, 2009, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Productos Marinos Del Norte

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 16-105red listfresh and frozen
    Source

Questions about Productos Marinos Del Norte

Is Productos Marinos Del Norte on an FDA import alert?
Yes. As of October 26, 2026, Productos Marinos Del Norte is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for fresh and frozen; FDA published the listing on September 10, 2009.
Has FDA refused shipments from Productos Marinos Del Norte?
No FDA import refusals for Productos Marinos Del Norte appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Productos Marinos Del Norte's FEI number?
Productos Marinos Del Norte's FDA Establishment Identifier (FEI) is 1000208181.
Can shipments from Productos Marinos Del Norte still enter the U.S.?
Shipments of fresh and frozen from Productos Marinos Del Norte can be detained without physical examination under Import Alert 16-105; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectProductos Marinos Del Nort 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.