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Gyodongfood Co., Ltd.

FDA import alert and refusal historyOkcheon, South KoreaFEI 3034077754

Recorded by FDA as GYODONGFOOD CO., LTD.

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

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As of October 26, 2026, Gyodongfood Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 6, 2026, most often for no scheduled process filed (NO PROCESS).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Beef soup, plain · NO PROCESS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Gyodongfood Co., Ltd.

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

2026

  1. Import refusal
    Refused, Beef soup, plainNO PROCESSEntry U47-2604290-4
    Source

Refusal charges, in plain English

  • NO PROCESS1 refused line

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Gyodongfood Co., Ltd.

Is Gyodongfood Co., Ltd. on an FDA import alert?
No listing for Gyodongfood Co., Ltd. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
Has FDA refused shipments from Gyodongfood Co., Ltd.?
Yes. FDA refused 1 shipment line from Gyodongfood Co., Ltd. on July 6, 2026. The most recent, on July 6, 2026, was beef soup, plain, charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Gyodongfood Co., Ltd.'s shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
What is Gyodongfood Co., Ltd.'s FEI number?
Gyodongfood Co., Ltd.'s FDA Establishment Identifier (FEI) is 3034077754.

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Example subjectGyodongfood 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.