Tokyo Niitakaya Co. Ltd.

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.

• NEEDS FCE1 refused line

  Processor not registered for canned or acidified foods

  The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

• NO PROCESS1 refused line

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

• 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 Tokyo Niitakaya Co. Ltd.

Is Tokyo Niitakaya Co. Ltd. on an FDA import alert?

No listing for Tokyo Niitakaya 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 Tokyo Niitakaya Co. Ltd.?

Yes. FDA refused 1 shipment line from Tokyo Niitakaya Co. Ltd. on June 10, 2022. The most recent, on June 10, 2022, was ginger, whole (spice), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Tokyo Niitakaya Co. Ltd.'s shipments?

The most frequent charges are COLOR LBLG (artificial coloring not declared, 1 line) and NEEDS FCE (processor not registered for canned or acidified foods, 1 line).

What is Tokyo Niitakaya Co. Ltd.'s FEI number?

Tokyo Niitakaya Co. Ltd.'s FDA Establishment Identifier (FEI) is 3012222460.