Njardar
FDA import alert and refusal historyLeinoy, NorwayFEI 2000009714
As of October 25, 2026, Njardar (Leinoy, Norway) is on the red list of FDA Import Alert 16-119 (Fish products from importer and processor combinations) for golden smoked herring, published by FDA on September 23, 2016, is also listed on Import Alert 16-120 (red list), 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 listIA 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Njardar
3 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 16-119red listGolden Smoked HerringSource
2011
- Import alert listingListed on Import Alert 16-120red listSalted Herring Products; Smoked Herring Products; Herring RoeSource
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Njardar
- Is Njardar on an FDA import alert?
- Yes. As of October 25, 2026, Njardar is on the red list of FDA Import Alert 16-119, “Fish products from importer and processor combinations”, for golden smoked herring; FDA published the listing on September 23, 2016.
- Has FDA refused shipments from Njardar?
- No FDA import refusals for Njardar appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Njardar last inspected by FDA?
- FDA's most recent inspection of Njardar with a final classification is dated March 15, 2011 and was classified OAI (Official Action Indicated).
- What is Njardar's FEI number?
- Njardar's FDA Establishment Identifier (FEI) is 2000009714.
- Can shipments from Njardar still enter the U.S.?
- Shipments of golden smoked herring from Njardar 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).
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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.