SupplierRadar

Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd

FDA import alert and refusal historyGanzhou, ChinaFEI 3036535835

Recorded by FDA as JIANGXI GANZHOU XINGWANJIA MODERN AGRICULTURAL DEVELOPMENT CO.,LTD

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectJiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Lt added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 27, 2026, Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between December 15, 2025 and February 2, 2026, most often for listeria monocytogenes (LISTERIA).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Fungus, white, whole (button) (fungi) · LABELING
Last warning letter
None found
Last inspection
None on record

Every FDA record for Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd

4 records, newest first. Each line links to the FDA page it came from.

2026

  1. Import refusal
    Refused, Fungus, white, whole (button) (fungi)LABELINGEntry DU7-0143004-1
    Source
  2. Import refusal
    Refused, 2 lines in one entry: EnokitakeLISTERIAEntry DU7-0142864-9Show 2 lines
    Source

2025

  1. Import refusal
    Refused, Fungus, white, whole (button) (fungi)LISTERIAEntry DU7-0143055-3
    Source

Refusal charges, in plain English

  • LISTERIA3 refused lines

    Listeria monocytogenes

    The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

  • LABELING1 refused line

    Fair Packaging and Labeling Act

    The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

Questions about Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd

Is Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd on an FDA import alert?
No listing for Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the China page.
Has FDA refused shipments from Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd?
Yes. FDA refused 4 shipment lines from Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd between December 15, 2025 and February 2, 2026. The most recent, on February 2, 2026, was fungus, white, whole (button) (fungi), charged as LABELING (fair packaging and labeling act).
Why did FDA refuse Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd's shipments?
The most frequent charges are LISTERIA (listeria monocytogenes, 3 lines) and LABELING (fair packaging and labeling act, 1 line).
What is Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd's FEI number?
Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd's FDA Establishment Identifier (FEI) is 3036535835.

Buying from Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Jiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Ltd.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectJiangxi Ganzhou Xingwanjia Modern Agricultural Development Co.,Lt added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.