Kawan Food (Nantong)
FDA import alert and refusal historyNantong, ChinaFEI 3007781996
As of October 26, 2026, Kawan Food (Nantong) is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on August 7, 2017, most often for melamine (MELAMINE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Bread/rolls/buns, n.e.c. · MELAMINE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Kawan Food (Nantong)
3 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
2017
Refusal charges, in plain English
- MELAMINE2 refused lines
Melamine
The product appeared to contain melamine or a melamine analog, which is an unsafe food additive within the meaning of section 409 of the FD&C Act.
Questions about Kawan Food (Nantong)
- Is Kawan Food (Nantong) on an FDA import alert?
- No listing for Kawan Food (Nantong) 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 Kawan Food (Nantong)?
- Yes. FDA refused 2 shipment lines from Kawan Food (Nantong) on August 7, 2017. The most recent, on August 7, 2017, was bread/rolls/buns, n.e.c., charged as MELAMINE (melamine).
- Why did FDA refuse Kawan Food (Nantong)'s shipments?
- The most frequent charge is MELAMINE (melamine, 2 lines).
- When was Kawan Food (Nantong) last inspected by FDA?
- FDA's most recent inspection of Kawan Food (Nantong) with a final classification is dated June 21, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Kawan Food (Nantong)'s FEI number?
- Kawan Food (Nantong)'s FDA Establishment Identifier (FEI) is 3007781996.
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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.