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Maeil Foods Co., Ltd.

FDA import alert and refusal historySuncheon, South KoreaFEI 3011149350

Recorded by FDA as MAEIL FOODS CO., LTD.

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

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As of October 26, 2026, Maeil Foods Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between April 29, 2022 and July 26, 2022, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Sauces, n.e.c. · LIST INGRE
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Maeil Foods Co., Ltd.

3 records, newest first. Each line links to the FDA page it came from.

2022

  1. Import refusal
    Refused, Sauces, n.e.c.LIST INGRELACKS N/CNO ENGLISHNUTRIT LBLNEEDS FCENO PROCESSEntry EPM-0168239-8
    Source
  2. Import refusal
    Refused, Pepper, hot, dried or pasteFILTHYEntry EUG-0025351-8
    Source

2016

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • LIST INGRE1 refused line

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

  • NEEDS FCE1 refused line

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • NO ENGLISH1 refused line

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • 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.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Maeil Foods Co., Ltd.

Is Maeil Foods Co., Ltd. on an FDA import alert?
No listing for Maeil Foods 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 Maeil Foods Co., Ltd.?
Yes. FDA refused 2 shipment lines from Maeil Foods Co., Ltd. between April 29, 2022 and July 26, 2022. The most recent, on July 26, 2022, was sauces, n.e.c., charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Maeil Foods Co., Ltd.'s shipments?
The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 1 line) and LACKS N/C (net quantity statement missing, 1 line).
When was Maeil Foods Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Maeil Foods Co., Ltd. with a final classification is dated May 24, 2016 and was classified VAI (Voluntary Action Indicated).
What is Maeil Foods Co., Ltd.'s FEI number?
Maeil Foods Co., Ltd.'s FDA Establishment Identifier (FEI) is 3011149350.

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Example subjectMaeil Foods 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.