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Cermaq Chile S.A.

FDA import alert and refusal historyPuerto Montt, ChileFEI 3009975801

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Example subjectCermaq Chile S.A added to Import Alert 16-129 (red list)

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As of October 25, 2026, Cermaq Chile 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 Cermaq Chile S.A.

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

2022

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

2014

  1. Import alert listing
    Listed on Import Alert 16-125green listVacuum Packaged Salmon
    Source

2011

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

Questions about Cermaq Chile S.A.

Is Cermaq Chile S.A. on an FDA import alert?
Yes. As of October 25, 2026, Cermaq Chile S.A. is on the green list of FDA Import Alert 16-125, “Refrigerated raw fish in reduced oxygen packaging”, for vacuum packaged salmon; FDA published the listing on November 3, 2014.
Has FDA refused shipments from Cermaq Chile S.A.?
No FDA import refusals for Cermaq Chile S.A. appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Cermaq Chile S.A. last inspected by FDA?
FDA's most recent inspection of Cermaq Chile S.A. with a final classification is dated August 16, 2022 and was classified VAI (Voluntary Action Indicated).
What is Cermaq Chile S.A.'s FEI number?
Cermaq Chile S.A.'s FDA Establishment Identifier (FEI) is 3009975801.

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Example subjectCermaq Chile 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.