Dardanel Onentas Gida San AS
FDA import alert and refusal historyCanakkale, TurkeyFEI 3010194056
Recorded by FDA as DARDANEL ONENTAS GIDA SAN AS
As of October 26, 2026, Dardanel Onentas Gida San AS (Canakkale, Turkey) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for cooked shrimp, published by FDA on March 13, 2009, 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 VAI (Voluntary Action Indicated)
Every FDA record for Dardanel Onentas Gida San AS
2 records, newest first. Each line links to the FDA page it came from.
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 16-39red listCooked shrimpSource
Questions about Dardanel Onentas Gida San AS
- Is Dardanel Onentas Gida San AS on an FDA import alert?
- Yes. As of October 26, 2026, Dardanel Onentas Gida San AS is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for cooked shrimp; FDA published the listing on March 13, 2009.
- Has FDA refused shipments from Dardanel Onentas Gida San AS?
- No FDA import refusals for Dardanel Onentas Gida San AS appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Dardanel Onentas Gida San AS last inspected by FDA?
- FDA's most recent inspection of Dardanel Onentas Gida San AS with a final classification is dated August 26, 2014 and was classified VAI (Voluntary Action Indicated).
- What is Dardanel Onentas Gida San AS's FEI number?
- Dardanel Onentas Gida San AS's FDA Establishment Identifier (FEI) is 3010194056.
- Can shipments from Dardanel Onentas Gida San AS still enter the U.S.?
- Shipments of cooked shrimp from Dardanel Onentas Gida San AS 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.