Bakkafrost Processing
FDA import alert and refusal historyGlyvrar, Faroe IslandsFEI 3010740901
As of October 25, 2026, Bakkafrost Processing (Glyvrar, Faroe Islands) is on the red list of FDA Import Alert 16-119 (Fish products from importer and processor combinations) for fresh ready-to-eat (rte) salmon (aquaculture), published by FDA on September 15, 2026, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-119 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Bakkafrost Processing
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 16-119red listFresh Ready-to-Eat (RTE) Salmon (Aquaculture)Source
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Bakkafrost Processing
- Is Bakkafrost Processing on an FDA import alert?
- Yes. As of October 25, 2026, Bakkafrost Processing is on the red list of FDA Import Alert 16-119, “Fish products from importer and processor combinations”, for fresh ready-to-eat (rte) salmon (aquaculture); FDA published the listing on September 15, 2026.
- Has FDA refused shipments from Bakkafrost Processing?
- No FDA import refusals for Bakkafrost Processing appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Bakkafrost Processing last inspected by FDA?
- FDA's most recent inspection of Bakkafrost Processing with a final classification is dated September 3, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Bakkafrost Processing's FEI number?
- Bakkafrost Processing's FDA Establishment Identifier (FEI) is 3010740901.
- Can shipments from Bakkafrost Processing still enter the U.S.?
- Shipments of fresh ready-to-eat (rte) salmon (aquaculture) from Bakkafrost Processing can be detained without physical examination under Import Alert 16-119; 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).
Buying from Bakkafrost Processing?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.