Is Umeken Toyama Factory on an FDA import alert?

No listing for Umeken Toyama 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 Umeken Toyama Factory?

Yes. FDA refused 2 shipment lines from Umeken Toyama Factory between October 31, 2016 and November 1, 2016. The most recent, on November 1, 2016, was vitamin c (ascorbic acid), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Umeken Toyama Factory's shipments?

The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 2 lines).

What is Umeken Toyama Factory's FEI number?

Umeken Toyama Factory's FDA Establishment Identifier (FEI) is 3012234985.

Umeken Toyama Factory

FDA import alert and refusal historyToyama, JapanFEI 3012234985

Recorded by FDA as UMEKEN TOYAMA FACTORY

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As of October 26, 2026, Umeken Toyama Factory is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between October 31, 2016 and November 1, 2016, 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: Nov 1, 2016Vitamin c (ascorbic acid) · UNSAFE COL
Last warning letter: None found
Last inspection: None on record

Every FDA record for Umeken Toyama Factory

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

2016

Nov 1, 2016Import refusal
Refused, Vitamin c (ascorbic acid)UNSAFE COLEntry BVU-0172892-5
Source
Oct 31, 2016Import refusal
Refused, Vitamin c (ascorbic acid)UNSAFE COLEntry BVU-0172892-5
Source

Refusal charges, in plain English

UNSAFE COL2 refused lines
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 Umeken Toyama Factory

Is Umeken Toyama Factory on an FDA import alert?: No listing for Umeken Toyama 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 Umeken Toyama Factory?: Yes. FDA refused 2 shipment lines from Umeken Toyama Factory between October 31, 2016 and November 1, 2016. The most recent, on November 1, 2016, was vitamin c (ascorbic acid), charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Umeken Toyama Factory's shipments?: The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 2 lines).
What is Umeken Toyama Factory's FEI number?: Umeken Toyama Factory's FDA Establishment Identifier (FEI) is 3012234985.

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