Vinsi International
FDA import alert and refusal historyAhmedabad, IndiaFEI 3033604935
Recorded by FDA as VINSI INTERNATIONAL
As of October 26, 2026, Vinsi International is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between July 9, 2025 and July 25, 2025, most often for food additive unsafe under section 409 (UNSAFE ADD).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Betel nut, paste · UNSAFE ADD
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Vinsi International
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Betel nut, pasteUNSAFE ADDEntry B4S-1011803-0Source
- Import refusalRefused, Betel nut, pasteUNSAFE ADDEntry B4S-1011718-0Source
Refusal charges, in plain English
- UNSAFE ADD2 refused lines
Food additive unsafe under section 409
The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.
Questions about Vinsi International
- Is Vinsi International on an FDA import alert?
- No listing for Vinsi International appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Vinsi International?
- Yes. FDA refused 2 shipment lines from Vinsi International between July 9, 2025 and July 25, 2025. The most recent, on July 25, 2025, was betel nut, paste, charged as UNSAFE ADD (food additive unsafe under section 409).
- Why did FDA refuse Vinsi International's shipments?
- The most frequent charge is UNSAFE ADD (food additive unsafe under section 409, 2 lines).
- What is Vinsi International's FEI number?
- Vinsi International's FDA Establishment Identifier (FEI) is 3033604935.
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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.