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Oyang Fisheries Co., Ltd.

FDA import alert and refusal historySeoul, South KoreaFEI 13988

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Example subjectOyang Fisheries Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Oyang Fisheries Co., Ltd. (Seoul, South Korea) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for fish roe, fishery products, n.e.c., 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 Oyang Fisheries Co., Ltd.

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 listFish Roe, Fishery Products, n.e.c.
    Source

Questions about Oyang Fisheries Co., Ltd.

Is Oyang Fisheries Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Oyang Fisheries Co., Ltd. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for fish roe, fishery products, n.e.c.; FDA published the listing on March 13, 2009.
Has FDA refused shipments from Oyang Fisheries Co., Ltd.?
No FDA import refusals for Oyang Fisheries Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Oyang Fisheries Co., Ltd.'s FEI number?
Oyang Fisheries Co., Ltd.'s FDA Establishment Identifier (FEI) is 13988.
Can shipments from Oyang Fisheries Co., Ltd. still enter the U.S.?
Shipments of fish roe, fishery products, n.e.c. from Oyang Fisheries Co., Ltd. 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 subjectOyang Fisheries Co., Ltd 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.