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Tokyo Shokuhin Sangyo Co., Ltd.

FDA import alert and refusal historySano, JapanFEI 3004298055

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Example subjectTokyo Shokuhin Sangyo Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Tokyo Shokuhin Sangyo Co., Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 18, 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 Tokyo Shokuhin Sangyo Co., Ltd.

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

2012

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

Questions about Tokyo Shokuhin Sangyo Co., Ltd.

Is Tokyo Shokuhin Sangyo Co., Ltd. on an FDA import alert?
No listing for Tokyo Shokuhin Sangyo Co., Ltd. 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 Tokyo Shokuhin Sangyo Co., Ltd.?
No FDA import refusals for Tokyo Shokuhin Sangyo Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Tokyo Shokuhin Sangyo Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Tokyo Shokuhin Sangyo Co., Ltd. with a final classification is dated June 18, 2018 and was classified NAI (No Action Indicated).
What is Tokyo Shokuhin Sangyo Co., Ltd.'s FEI number?
Tokyo Shokuhin Sangyo Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004298055.

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Example subjectTokyo Shokuhin Sangyo Co., Ltd 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.