Kikkoman Food Tech Company Main Plant
FDA import alert and refusal historyNoda, JapanFEI 3004319532
As of October 26, 2026, Kikkoman Food Tech Company Main Plant has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on November 8, 2019, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)
Every FDA record for Kikkoman Food Tech Company Main Plant
2 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2013
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Kikkoman Food Tech Company Main Plant
- Is Kikkoman Food Tech Company Main Plant on an FDA import alert?
- No listing for Kikkoman Food Tech Company Main 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 Kikkoman Food Tech Company Main Plant?
- No FDA import refusals for Kikkoman Food Tech Company Main Plant appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Kikkoman Food Tech Company Main Plant last inspected by FDA?
- FDA's most recent inspection of Kikkoman Food Tech Company Main Plant with a final classification is dated November 8, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Kikkoman Food Tech Company Main Plant's FEI number?
- Kikkoman Food Tech Company Main Plant's FDA Establishment Identifier (FEI) is 3004319532.
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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.