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Ottogi Ramen Co., Ltd.

FDA import alert and refusal historyPyungtaek, Kyungki, South KoreaFEI 1000411455

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

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As of October 25, 2026, Ottogi Ramen Co., Ltd. (Pyungtaek, Kyungki, South Korea) is on the red list of FDA Import Alert 99-36 (Low-acid canned/acidified foods: process information) for black bean sauce; hash sauce, published by FDA on June 3, 2014, 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 Ottogi Ramen Co., Ltd.

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

2014

  1. Import alert listing
    Listed on Import Alert 99-36red listBlack bean sauce; hash sauce
    Source

Questions about Ottogi Ramen Co., Ltd.

Is Ottogi Ramen Co., Ltd. on an FDA import alert?
Yes. As of October 25, 2026, Ottogi Ramen Co., Ltd. is on the red list of FDA Import Alert 99-36, “Low-acid canned/acidified foods: process information”, for black bean sauce; hash sauce; FDA published the listing on June 3, 2014.
Has FDA refused shipments from Ottogi Ramen Co., Ltd.?
No FDA import refusals for Ottogi Ramen Co., Ltd. appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Ottogi Ramen Co., Ltd.'s FEI number?
Ottogi Ramen Co., Ltd.'s FDA Establishment Identifier (FEI) is 1000411455.
Can shipments from Ottogi Ramen Co., Ltd. still enter the U.S.?
Shipments of black bean sauce; hash sauce from Ottogi Ramen Co., Ltd. can be detained without physical examination under Import Alert 99-36; 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 subjectOttogi Ramen 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.