Cixi Vegtables Development Co.,
FDA import alert and refusal historyZhejiang, ChinaFEI 3015271414
Recorded by FDA as CIXI VEGTABLES DEVELOPMENT CO.,
As of October 26, 2026, Cixi Vegtables Development Co., is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 8, 2026, most often for imptrhaccp (IMPTRHACCP).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Oysters · IMPTRHACCP
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Cixi Vegtables Development Co.,
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, OystersIMPTRHACCPMFR INSANEntry U47-2511801-0Source
Refusal charges, in plain English
- IMPTRHACCP1 refused line
IMPTRHACCP
- MFR INSAN1 refused line
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
Questions about Cixi Vegtables Development Co.,
- Is Cixi Vegtables Development Co., on an FDA import alert?
- No listing for Cixi Vegtables Development Co., 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 Cixi Vegtables Development Co.,?
- Yes. FDA refused 1 shipment line from Cixi Vegtables Development Co., on January 8, 2026. The most recent, on January 8, 2026, was oysters, charged as IMPTRHACCP (imptrhaccp).
- Why did FDA refuse Cixi Vegtables Development Co.,'s shipments?
- The most frequent charges are IMPTRHACCP (imptrhaccp, 1 line) and MFR INSAN (insanitary manufacturing, processing or packing, 1 line).
- What is Cixi Vegtables Development Co.,'s FEI number?
- Cixi Vegtables Development Co.,'s FDA Establishment Identifier (FEI) is 3015271414.
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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.