Viciumai Ir Partneriai
FDA import alert and refusal historyPlunge, LithuaniaFEI 3010007579
As of October 26, 2026, Viciumai Ir Partneriai (Plunge, Lithuania) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for herring, published by FDA on June 7, 2010, 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 16-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Viciumai Ir Partneriai
3 records, newest first. Each line links to the FDA page it came from.
2024
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2019
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2010
- Import alert listingListed on Import Alert 16-39red listHerringSource
Questions about Viciumai Ir Partneriai
- Is Viciumai Ir Partneriai on an FDA import alert?
- Yes. As of October 26, 2026, Viciumai Ir Partneriai is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for herring; FDA published the listing on June 7, 2010.
- Has FDA refused shipments from Viciumai Ir Partneriai?
- No FDA import refusals for Viciumai Ir Partneriai appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Viciumai Ir Partneriai last inspected by FDA?
- FDA's most recent inspection of Viciumai Ir Partneriai with a final classification is dated July 31, 2024 and was classified NAI (No Action Indicated).
- What is Viciumai Ir Partneriai's FEI number?
- Viciumai Ir Partneriai's FDA Establishment Identifier (FEI) is 3010007579.
- Can shipments from Viciumai Ir Partneriai still enter the U.S.?
- Shipments of herring from Viciumai Ir Partneriai can be detained without physical examination under Import Alert 16-39; 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.