Meito Sangyo Co., Ltd

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

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 Meito Sangyo Co., Ltd

Is Meito Sangyo Co., Ltd on an FDA import alert?

No listing for Meito Sangyo 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 Meito Sangyo Co., Ltd?

Yes. FDA refused 1 shipment line from Meito Sangyo Co., Ltd on April 9, 2019. The most recent, on April 9, 2019, was beverage base not mentioned elsewhere, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).

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

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

When was Meito Sangyo Co., Ltd last inspected by FDA?

FDA's most recent inspection of Meito Sangyo Co., Ltd with a final classification is dated April 4, 2025 and was classified VAI (Voluntary Action Indicated).

What is Meito Sangyo Co., Ltd's FEI number?

Meito Sangyo Co., Ltd's FDA Establishment Identifier (FEI) is 3024202259.