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Jiangmen City Xin Qu Shi Trading Ltd

FDA import alert and refusal historyJiangmen, ChinaFEI 3013301460

Recorded by FDA as JIANGMEN CITY XIN QU SHI TRADING LTD

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Example subjectJiangmen City Xin Qu Shi Trading Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jiangmen City Xin Qu Shi Trading Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between December 20, 2016 and April 6, 2017, most often for color additive unsafe under section 721 (UNSAFE COL).

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

Current status

Import alerts
Not listed
Last import refusal
Noodles and noodle products, n.e.c. · UNSAFE COL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Jiangmen City Xin Qu Shi Trading Ltd

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

2017

  1. Import refusal
    Refused, 4 lines in one entry: Noodles and noodle products, n.e.c.UNSAFE COLEntry 9EH-0015832-1Show 4 lines
    Source

2016

  1. Import refusal
    Refused, Plain cookies,biscuits and wafers, n.e.c.POISONOUSMELAMINEUNFIT4FOODLABELINGNUTRIT LBLEntry 9EH-0013579-0
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Fungi products not mentioned elsewhere, n.e.c.FILTHYEntry 9EH-0013579-0Show 2 lines
    • Refused, Fungi products not mentioned elsewhere, n.e.c.FILTHYEntry 9EH-0013579-0Source
    • Refused, Fungi products not mentioned elsewhere, n.e.c.FILTHYEntry 9EH-0013579-0Source
    Source

Refusal charges, in plain English

  • UNSAFE COL4 refused lines

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

  • FILTHY2 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

  • 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.

  • MELAMINE1 refused line

    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.

  • NUTRIT LBL1 refused line

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • POISONOUS1 refused line

    Poisonous or deleterious substance

    The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.

  • UNFIT4FOOD1 refused line

    Unfit for food

    The product appeared to be unfit for food.

Questions about Jiangmen City Xin Qu Shi Trading Ltd

Is Jiangmen City Xin Qu Shi Trading Ltd on an FDA import alert?
No listing for Jiangmen City Xin Qu Shi Trading 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 Jiangmen City Xin Qu Shi Trading Ltd?
Yes. FDA refused 7 shipment lines from Jiangmen City Xin Qu Shi Trading Ltd between December 20, 2016 and April 6, 2017. The most recent, on April 6, 2017, was noodles and noodle products, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
Why did FDA refuse Jiangmen City Xin Qu Shi Trading Ltd's shipments?
The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 4 lines) and FILTHY (filthy, putrid or decomposed substance, 2 lines).
What is Jiangmen City Xin Qu Shi Trading Ltd's FEI number?
Jiangmen City Xin Qu Shi Trading Ltd's FDA Establishment Identifier (FEI) is 3013301460.

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Example subjectJiangmen City Xin Qu Shi Trading Lt added to Import Alert 16-129 (red list)

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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.