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Norway Seafoods Baatsfjord AS

FDA import alert and refusal historyBaatsfjord, NorwayFEI 3004302190

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Example subjectNorway Seafoods Baatsfjord A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Norway Seafoods Baatsfjord AS has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 14, 2016, 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 Norway Seafoods Baatsfjord AS

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

2016

  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 Norway Seafoods Baatsfjord AS

Is Norway Seafoods Baatsfjord AS on an FDA import alert?
No listing for Norway Seafoods Baatsfjord AS appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Norway page.
Has FDA refused shipments from Norway Seafoods Baatsfjord AS?
No FDA import refusals for Norway Seafoods Baatsfjord AS appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Norway Seafoods Baatsfjord AS last inspected by FDA?
FDA's most recent inspection of Norway Seafoods Baatsfjord AS with a final classification is dated June 14, 2016 and was classified VAI (Voluntary Action Indicated).
What is Norway Seafoods Baatsfjord AS's FEI number?
Norway Seafoods Baatsfjord AS's FDA Establishment Identifier (FEI) is 3004302190.

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Example subjectNorway Seafoods Baatsfjord 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.