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Maruka Co., Ltd.

FDA import alert and refusal historyToyota, JapanFEI 1000210619

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

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As of October 26, 2026, Maruka Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 3, 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
Burdock, gobo (root & tuber vegetable) · UNSAFE COL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Maruka Co., Ltd.

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

2026

  1. Import refusal
    Refused, Burdock, gobo (root & tuber vegetable)UNSAFE COLEntry AQ1-7049768-2
    Source

Refusal charges, in plain English

  • 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 Maruka Co., Ltd.

Is Maruka Co., Ltd. on an FDA import alert?
No listing for Maruka 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 Maruka Co., Ltd.?
Yes. FDA refused 1 shipment line from Maruka Co., Ltd. on March 3, 2026. The most recent, on March 3, 2026, was burdock, gobo (root & tuber vegetable), charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Maruka Co., Ltd.'s shipments?
The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
What is Maruka Co., Ltd.'s FEI number?
Maruka Co., Ltd.'s FDA Establishment Identifier (FEI) is 1000210619.

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Example subjectMaruka 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.