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Salmones Blumar S.A.

FDA import alert and refusal historyTalcahuano, ChileFEI 1000158066

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Example subjectSalmones Blumar S.A added to Import Alert 16-129 (red list)

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As of October 25, 2026, Salmones Blumar S.A. is on the green list of FDA Import Alert 16-125, which exempts its listed products from detention without physical examination under that alert, 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
Classified VAI (Voluntary Action Indicated)

Every FDA record for Salmones Blumar S.A.

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

2015

  1. Import alert listing
    Listed on Import Alert 16-125green listSalmon Humpback; Silver; King; Sockeye; Etc; Vacuum Packaged Atlantic Salmon
    Source

2012

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

Questions about Salmones Blumar S.A.

Is Salmones Blumar S.A. on an FDA import alert?
Yes. As of October 25, 2026, Salmones Blumar S.A. is on the green list of FDA Import Alert 16-125, “Refrigerated raw fish in reduced oxygen packaging”, for salmon humpback; silver; king; sockeye; etc; vacuum packaged atlantic salmon; FDA published the listing on June 25, 2015.
Has FDA refused shipments from Salmones Blumar S.A.?
No FDA import refusals for Salmones Blumar S.A. appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Salmones Blumar S.A. last inspected by FDA?
FDA's most recent inspection of Salmones Blumar S.A. with a final classification is dated April 26, 2012 and was classified VAI (Voluntary Action Indicated).
What is Salmones Blumar S.A.'s FEI number?
Salmones Blumar S.A.'s FDA Establishment Identifier (FEI) is 1000158066.

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Example subjectSalmones Blumar 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.