SupplierRadar

Yoshina Inc

FDA import alert and refusal historyNishio, JapanFEI 3013214298

Recorded by FDA as YOSHINA INC

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Example subjectYoshina In added to Import Alert 16-129 (red list)

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As of October 26, 2026, Yoshina Inc is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 28, 2017, 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
Pudding (pie filling) mix, n.e.c. (not custard) · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Yoshina Inc

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

2017

  1. Import refusal
    Refused, Pudding (pie filling) mix, n.e.c. (not custard)NO ENGLISHEntry UPS-2104378-2
    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 Yoshina Inc

Is Yoshina Inc on an FDA import alert?
No listing for Yoshina 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 Yoshina Inc?
Yes. FDA refused 1 shipment line from Yoshina Inc on February 28, 2017. The most recent, on February 28, 2017, was pudding (pie filling) mix, n.e.c. (not custard), charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Yoshina Inc's shipments?
The most frequent charge is NO ENGLISH (required label information not in english, 1 line).
What is Yoshina Inc's FEI number?
Yoshina Inc's FDA Establishment Identifier (FEI) is 3013214298.

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Example subjectYoshina In 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.