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Akita Shokusan, Co., Ltd

FDA import alert and refusal historySemboku-Gun Misato-Ch, JapanFEI 3030149628

Recorded by FDA as AKITA SHOKUSAN, CO., LTD

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Example subjectAkita Shokusan, Co., Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Akita Shokusan, Co., Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between August 5, 2025 and October 2, 2026, most often for color additive unsafe under section 721 (UNSAFE COL).

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

Current status

Import alerts
Not listed
Last import refusal
Ginger root (root & tuber vegetable) · UNSAFE COL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Akita Shokusan, Co., Ltd

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

2026

  1. Import refusal
    Refused, 2 lines in one entry: Ginger root (root & tuber vegetable)UNSAFE COLEntry K64-3065975-0Show 2 lines
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Ginger root (root & tuber vegetable)UNSAFE COLEntry K64-3065334-0Show 2 lines
    Source

2025

  1. Import refusal
    Refused, Radish (root & tuber vegetable)UNSAFE COLCOLOR LBLGEntry K64-3061401-1
    Source
  2. Import refusal
    Refused, Radish (root & tuber vegetable)UNSAFE COLCOLOR LBLGEntry K64-3059978-2
    Source

Refusal charges, in plain English

  • UNSAFE COL6 refused lines

    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.

  • COLOR LBLG2 refused lines

    Artificial coloring not declared

    The product appeared to contain an artificial coloring without labeling that states that fact.

Questions about Akita Shokusan, Co., Ltd

Is Akita Shokusan, Co., Ltd on an FDA import alert?
No listing for Akita Shokusan, 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 Japan page.
Has FDA refused shipments from Akita Shokusan, Co., Ltd?
Yes. FDA refused 6 shipment lines from Akita Shokusan, Co., Ltd between August 5, 2025 and October 2, 2026. The most recent, on October 2, 2026, was ginger root (root & tuber vegetable), charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Akita Shokusan, Co., Ltd's shipments?
The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 6 lines) and COLOR LBLG (artificial coloring not declared, 2 lines).
What is Akita Shokusan, Co., Ltd's FEI number?
Akita Shokusan, Co., Ltd's FDA Establishment Identifier (FEI) is 3030149628.

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Example subjectAkita Shokusan, Co., Lt 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.