SupplierRadar

Sanuki Kanzume Co., Mino Plant

FDA import alert and refusal historyMitoyo, JapanFEI 3003244067

Recorded by FDA as SANUKI KANZUME CO., MINO PLANT

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Example subjectSanuki Kanzume Co., Mino Plan added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sanuki Kanzume Co., Mino Plant has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on February 23, 2018, was classified NAI (No Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Sanuki Kanzume Co., Mino Plant

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

2018

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2010

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Questions about Sanuki Kanzume Co., Mino Plant

Is Sanuki Kanzume Co., Mino Plant on an FDA import alert?
No listing for Sanuki Kanzume Co., Mino Plant 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 Sanuki Kanzume Co., Mino Plant?
No FDA import refusals for Sanuki Kanzume Co., Mino Plant appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Sanuki Kanzume Co., Mino Plant last inspected by FDA?
FDA's most recent inspection of Sanuki Kanzume Co., Mino Plant with a final classification is dated February 23, 2018 and was classified NAI (No Action Indicated).
What is Sanuki Kanzume Co., Mino Plant's FEI number?
Sanuki Kanzume Co., Mino Plant's FDA Establishment Identifier (FEI) is 3003244067.

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Example subjectSanuki Kanzume Co., Mino Plan 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.