Brivais Vilnis
FDA import alert and refusal historySalacgriva, LatviaFEI 3002668627
As of October 26, 2026, Brivais Vilnis (Salacgriva, Latvia) is on the red list of FDA Import Alert 16-119 (Fish products from importer and processor combinations) for canned mackerel in tomato sauce, published by FDA on August 31, 2016, 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 OAI (Official Action Indicated)
Every FDA record for Brivais Vilnis
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 16-119red listCanned Mackerel in Tomato sauceSource
2015
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Brivais Vilnis
- Is Brivais Vilnis on an FDA import alert?
- Yes. As of October 26, 2026, Brivais Vilnis is on the red list of FDA Import Alert 16-119, “Fish products from importer and processor combinations”, for canned mackerel in tomato sauce; FDA published the listing on August 31, 2016.
- Has FDA refused shipments from Brivais Vilnis?
- No FDA import refusals for Brivais Vilnis appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Brivais Vilnis last inspected by FDA?
- FDA's most recent inspection of Brivais Vilnis with a final classification is dated May 13, 2015 and was classified OAI (Official Action Indicated).
- What is Brivais Vilnis's FEI number?
- Brivais Vilnis's FDA Establishment Identifier (FEI) is 3002668627.
- Can shipments from Brivais Vilnis still enter the U.S.?
- Shipments of canned mackerel in tomato sauce from Brivais Vilnis 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.