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

No listing for Kinjoseika 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 Kinjoseika Co., Ltd.?

Yes. FDA refused 1 shipment line from Kinjoseika Co., Ltd. on June 25, 2018. The most recent, on June 25, 2018, was imitation fruit, jam, jelly, preserves, marmalade, butter or candied, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).

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

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

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

FDA's most recent inspection of Kinjoseika Co., Ltd. with a final classification is dated April 17, 2024 and was classified NAI (No Action Indicated).

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

Kinjoseika Co., Ltd.'s FDA Establishment Identifier (FEI) is 3012349011.

Kinjoseika Co., Ltd.

FDA import alert and refusal historyToyohashi, JapanFEI 3012349011

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As of October 26, 2026, Kinjoseika Co., Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 25, 2018, most often for color additive unsafe under section 721 (UNSAFE COL).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Jun 25, 2018Imitation fruit, jam, jelly, preserves, marmalade, butter or candied, n.e.c. · UNSAFE COL
Last warning letter: None found
Last inspection: Apr 17, 2024Classified NAI (No Action Indicated)

Every FDA record for Kinjoseika Co., Ltd.

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

2024

Apr 17, 2024Inspection
Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
Source

2018

Jun 25, 2018Import refusal
Refused, Imitation fruit, jam, jelly, preserves, marmalade, butter or candied, n.e.c.UNSAFE COLEntry 9ES-0037821-4
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 Kinjoseika Co., Ltd.

Is Kinjoseika Co., Ltd. on an FDA import alert?: No listing for Kinjoseika 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 Kinjoseika Co., Ltd.?: Yes. FDA refused 1 shipment line from Kinjoseika Co., Ltd. on June 25, 2018. The most recent, on June 25, 2018, was imitation fruit, jam, jelly, preserves, marmalade, butter or candied, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Kinjoseika Co., Ltd.'s shipments?: The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
When was Kinjoseika Co., Ltd. last inspected by FDA?: FDA's most recent inspection of Kinjoseika Co., Ltd. with a final classification is dated April 17, 2024 and was classified NAI (No Action Indicated).
What is Kinjoseika Co., Ltd.'s FEI number?: Kinjoseika Co., Ltd.'s FDA Establishment Identifier (FEI) is 3012349011.

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