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Nakaura Shokuhin

FDA import alert and refusal historyMatsue, JapanFEI 3014690593

Recorded by FDA as NAKAURA SHOKUHIN

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Example subjectNakaura Shokuhi added to Import Alert 16-129 (red list)

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As of October 26, 2026, Nakaura Shokuhin is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on April 21, 2026, most often for poisonous or deleterious substance (ordinarily injurious) (POISONORD).

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

Current status

Import alerts
Not listed
Last import refusal
Puffer · POISONORD
Last warning letter
None found
Last inspection
None on record

Every FDA record for Nakaura Shokuhin

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

2026

  1. Import refusal
    Refused, PufferPOISONORDEntry 235-1760861-0
    Source

Refusal charges, in plain English

  • POISONORD1 refused line

    Poisonous or deleterious substance (ordinarily injurious)

    The product appeared to contain a poisonous or deleterious substance in a form or amount that would ordinarily render it injurious to health.

Questions about Nakaura Shokuhin

Is Nakaura Shokuhin on an FDA import alert?
No listing for Nakaura Shokuhin 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 Nakaura Shokuhin?
Yes. FDA refused 1 shipment line from Nakaura Shokuhin on April 21, 2026. The most recent, on April 21, 2026, was puffer, charged as POISONORD (poisonous or deleterious substance (ordinarily injurious)).
Why did FDA refuse Nakaura Shokuhin's shipments?
The most frequent charge is POISONORD (poisonous or deleterious substance (ordinarily injurious), 1 line).
What is Nakaura Shokuhin's FEI number?
Nakaura Shokuhin's FDA Establishment Identifier (FEI) is 3014690593.

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Example subjectNakaura Shokuhi 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.