Zhejiang Zheng Wanli Wines Co.,Ltd.
FDA import alert and refusal historyNingbo, ChinaFEI 3014125246
As of October 26, 2026, Zhejiang Zheng Wanli Wines Co.,Ltd. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between March 30, 2022 and April 6, 2022, most often for importer not in compliance with fsvp (FSVP VIO).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Sauces, n.e.c. · FSVP VIO
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Zhejiang Zheng Wanli Wines Co.,Ltd.
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FSVP VIO2 refused lines
Importer not in compliance with FSVP
The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.
Questions about Zhejiang Zheng Wanli Wines Co.,Ltd.
- Is Zhejiang Zheng Wanli Wines Co.,Ltd. on an FDA import alert?
- No listing for Zhejiang Zheng Wanli Wines 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 Zhejiang Zheng Wanli Wines Co.,Ltd.?
- Yes. FDA refused 2 shipment lines from Zhejiang Zheng Wanli Wines Co.,Ltd. between March 30, 2022 and April 6, 2022. The most recent, on April 6, 2022, was sauces, n.e.c., charged as FSVP VIO (importer not in compliance with fsvp).
- Why did FDA refuse Zhejiang Zheng Wanli Wines Co.,Ltd.'s shipments?
- The most frequent charge is FSVP VIO (importer not in compliance with fsvp, 2 lines).
- What is Zhejiang Zheng Wanli Wines Co.,Ltd.'s FEI number?
- Zhejiang Zheng Wanli Wines Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3014125246.
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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.