Is Ichibiki Co.,Ltd on an FDA import alert?

No listing for Ichibiki Co.,Ltd appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Japan page.

Has FDA refused shipments from Ichibiki Co.,Ltd?

Yes. FDA refused 1 shipment line from Ichibiki Co.,Ltd on December 21, 2018. The most recent, on December 21, 2018, was radish (root & tuber vegetable), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Ichibiki Co.,Ltd's shipments?

The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).

When was Ichibiki Co.,Ltd last inspected by FDA?

FDA's most recent inspection of Ichibiki Co.,Ltd with a final classification is dated February 14, 2014 and was classified VAI (Voluntary Action Indicated).

What is Ichibiki Co.,Ltd's FEI number?

Ichibiki Co.,Ltd's FDA Establishment Identifier (FEI) is 3008087776.

Ichibiki Co.,Ltd

FDA import alert and refusal historyTokai, JapanFEI 3008087776

Recorded by FDA as ICHIBIKI CO.,LTD

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As of October 25, 2026, Ichibiki Co.,Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 21, 2018, most often for color additive unsafe under section 721 (UNSAFE COL).

Data from FDA public records, last checked October 25, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Dec 21, 2018Radish (root & tuber vegetable) · UNSAFE COL
Last warning letter: None found
Last inspection: Feb 14, 2014Classified VAI (Voluntary Action Indicated)

Every FDA record for Ichibiki Co.,Ltd

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

2018

Dec 21, 2018Import refusal
Refused, Radish (root & tuber vegetable)UNSAFE COLEntry 221-6135159-2
Source

2014

Feb 14, 2014Inspection
Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
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 Ichibiki Co.,Ltd

Is Ichibiki Co.,Ltd on an FDA import alert?: No listing for Ichibiki Co.,Ltd appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Japan page.
Has FDA refused shipments from Ichibiki Co.,Ltd?: Yes. FDA refused 1 shipment line from Ichibiki Co.,Ltd on December 21, 2018. The most recent, on December 21, 2018, was radish (root & tuber vegetable), charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Ichibiki Co.,Ltd's shipments?: The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
When was Ichibiki Co.,Ltd last inspected by FDA?: FDA's most recent inspection of Ichibiki Co.,Ltd with a final classification is dated February 14, 2014 and was classified VAI (Voluntary Action Indicated).
What is Ichibiki Co.,Ltd's FEI number?: Ichibiki Co.,Ltd's FDA Establishment Identifier (FEI) is 3008087776.

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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.