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Kugi Foods Co., Ltd.

FDA import alert and refusal historyTainan City, TaiwanFEI 3011373650

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

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As of October 26, 2026, Kugi Foods Co., Ltd. (Tainan City, Taiwan) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for hokkaide flavor powder, published by FDA on March 22, 2019, is also listed on Import Alert 99-22 (red list), and has 3 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Gelatin, n.e.c. · MELAMINE
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Kugi Foods Co., Ltd.

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

2023

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2022

  1. Import refusal
    Refused, Gelatin, n.e.c.MELAMINEEntry B7V-0056810-3
    Source

2019

  1. Import alert listing
    Listed on Import Alert 99-39red listHokkaide flavor powder
    Source
  2. Import alert listing
    Listed on Import Alert 99-22red listHokkaide Flavor Powder (invoiced as Non-Dairy Creamer Powder); HOKKAIDE FLAVOR POWDER
    Source
  3. Import refusal
    Refused, 2 lines in one entry: Pudding (pie filling) mix, n.e.c. (not custard); Imitation milk, dried milk type productUNSAFE COLLIST INGRELACKS FIRMEntry W69-3572929-4Show 2 lines
    Source

Refusal charges, in plain English

  • LACKS FIRM1 refused line

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • 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).

  • MELAMINE1 refused line

    Melamine

    The product appeared to contain melamine or a melamine analog, which is an unsafe food additive within the meaning of section 409 of the FD&C Act.

  • UNSAFE COL1 refused line

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Kugi Foods Co., Ltd.

Is Kugi Foods Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Kugi Foods Co., Ltd. is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for hokkaide flavor powder; FDA published the listing on March 22, 2019.
Has FDA refused shipments from Kugi Foods Co., Ltd.?
Yes. FDA refused 3 shipment lines from Kugi Foods Co., Ltd. between January 11, 2019 and November 18, 2022. The most recent, on November 18, 2022, was gelatin, n.e.c., charged as MELAMINE (melamine).
Why did FDA refuse Kugi Foods Co., Ltd.'s shipments?
The most frequent charges are LACKS FIRM (manufacturer name and address missing, 1 line) and LIST INGRE (ingredients not listed, 1 line).
When was Kugi Foods Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Kugi Foods Co., Ltd. with a final classification is dated June 6, 2023 and was classified NAI (No Action Indicated).
What is Kugi Foods Co., Ltd.'s FEI number?
Kugi Foods Co., Ltd.'s FDA Establishment Identifier (FEI) is 3011373650.
Can shipments from Kugi Foods Co., Ltd. still enter the U.S.?
Shipments of hokkaide flavor powder from Kugi Foods Co., Ltd. can be detained without physical examination under Import Alert 99-39; 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 subjectKugi 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.