Kimura Tsukemono Miyazaki Kogyo K.K.

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

Refusal charges, in plain English

• COLOR LBLG2 refused lines

  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 Kimura Tsukemono Miyazaki Kogyo K.K.

Is Kimura Tsukemono Miyazaki Kogyo K.K. on an FDA import alert?

No listing for Kimura Tsukemono Miyazaki Kogyo K.K. 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 Kimura Tsukemono Miyazaki Kogyo K.K.?

Yes. FDA refused 2 shipment lines from Kimura Tsukemono Miyazaki Kogyo K.K. between December 9, 2024 and February 9, 2026. The most recent, on February 9, 2026, was radish (root & tuber vegetable), charged as COLOR LBLG (artificial coloring not declared).

Why did FDA refuse Kimura Tsukemono Miyazaki Kogyo K.K.'s shipments?

The most frequent charges are COLOR LBLG (artificial coloring not declared, 2 lines) and UNSAFE COL (color additive unsafe under section 721, 1 line).

When was Kimura Tsukemono Miyazaki Kogyo K.K. last inspected by FDA?

FDA's most recent inspection of Kimura Tsukemono Miyazaki Kogyo K.K. with a final classification is dated July 31, 2026 and was classified VAI (Voluntary Action Indicated).

What is Kimura Tsukemono Miyazaki Kogyo K.K.'s FEI number?

Kimura Tsukemono Miyazaki Kogyo K.K.'s FDA Establishment Identifier (FEI) is 3011192786.