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Sunkyong Limited

FDA import alert and refusal historySeoul, South KoreaFEI 1000284583

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Example subjectSunkyong Limite added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sunkyong Limited (Seoul, South Korea) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for crab; surimi (used for further processing into imitation seafood), 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

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Sunkyong Limited

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 16-39red listCrab; Surimi (Used for Further Processing into Imitation Seafood)
    Source

Questions about Sunkyong Limited

Is Sunkyong Limited on an FDA import alert?
Yes. As of October 26, 2026, Sunkyong Limited is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for crab; surimi (used for further processing into imitation seafood); FDA published the listing on March 13, 2009.
Has FDA refused shipments from Sunkyong Limited?
No FDA import refusals for Sunkyong Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Sunkyong Limited's FEI number?
Sunkyong Limited's FDA Establishment Identifier (FEI) is 1000284583.
Can shipments from Sunkyong Limited still enter the U.S.?
Shipments of crab; surimi (used for further processing into imitation seafood) from Sunkyong Limited 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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Example subjectSunkyong Limite added to Import Alert 16-129 (red list)

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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.