Ohori Co., Ltd. Nikko Factory

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

Refusal charges, in plain English

• COLOR LBLG1 refused line

  Artificial coloring not declared

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

• 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 Ohori Co., Ltd. Nikko Factory

Is Ohori Co., Ltd. Nikko Factory on an FDA import alert?

No listing for Ohori Co., Ltd. Nikko Factory 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 Ohori Co., Ltd. Nikko Factory?

Yes. FDA refused 1 shipment line from Ohori Co., Ltd. Nikko Factory on April 15, 2025. The most recent, on April 15, 2025, was ginger root (root & tuber vegetable), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Ohori Co., Ltd. Nikko Factory's shipments?

The most frequent charges are COLOR LBLG (artificial coloring not declared, 1 line) and UNSAFE COL (color additive unsafe under section 721, 1 line).

What is Ohori Co., Ltd. Nikko Factory's FEI number?

Ohori Co., Ltd. Nikko Factory's FDA Establishment Identifier (FEI) is 3009897991.