Tomo Foods Products Co., Ltd.
FDA import alert and refusal historyZhangzhou, ChinaFEI 3004334068
As of October 26, 2026, Tomo Foods Products Co., Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 21, 2022, 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 Tomo Foods Products Co., Ltd.
3 records, newest first. Each line links to the FDA page it came from.
2022
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2018
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Tomo Foods Products Co., Ltd.
- Is Tomo Foods Products Co., Ltd. on an FDA import alert?
- No listing for Tomo Foods Products 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 China page.
- Has FDA refused shipments from Tomo Foods Products Co., Ltd.?
- No FDA import refusals for Tomo Foods Products Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Tomo Foods Products Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Tomo Foods Products Co., Ltd. with a final classification is dated September 21, 2022 and was classified VAI (Voluntary Action Indicated).
- What is Tomo Foods Products Co., Ltd.'s FEI number?
- Tomo Foods Products Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004334068.
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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.