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Yichihiro, Inc.

FDA import alert and refusal historyYokohama, JapanFEI 3014535750

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Example subjectYichihiro, Inc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Yichihiro, Inc. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 27, 2019, most often for required label information not in english (NO ENGLISH).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Multiple food specialities, side dishes and desserts, n.e.c. · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Yichihiro, Inc.

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

2019

  1. Import refusal
    Refused, Multiple food specialities, side dishes and desserts, n.e.c.NO ENGLISHEntry 349-1006847-6
    Source

Refusal charges, in plain English

  • NO ENGLISH1 refused line

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

Questions about Yichihiro, Inc.

Is Yichihiro, Inc. on an FDA import alert?
No listing for Yichihiro, Inc. 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 Yichihiro, Inc.?
Yes. FDA refused 1 shipment line from Yichihiro, Inc. on June 27, 2019. The most recent, on June 27, 2019, was multiple food specialities, side dishes and desserts, n.e.c., charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Yichihiro, Inc.'s shipments?
The most frequent charge is NO ENGLISH (required label information not in english, 1 line).
What is Yichihiro, Inc.'s FEI number?
Yichihiro, Inc.'s FDA Establishment Identifier (FEI) is 3014535750.

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Example subjectYichihiro, Inc added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.