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Guanxian Ruichang Trading Co., Ltd

FDA import alert and refusal historyLiochngsh, ChinaFEI 3010406060

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Example subjectGuanxian Ruichang Trading Co., Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Guanxian Ruichang Trading Co., Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 11, 2022, most often for melamine (MELAMINE).

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

Current status

Import alerts
Not listed
Last import refusal
Wheat gluten · MELAMINE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Guanxian Ruichang Trading Co., Ltd

1 record, newest first. Each line links to the FDA page it came from.

2022

  1. Import refusal
    Refused, Wheat glutenMELAMINEEntry 879-4031948-3
    Source

Refusal charges, in plain English

  • 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.

Questions about Guanxian Ruichang Trading Co., Ltd

Is Guanxian Ruichang Trading Co., Ltd on an FDA import alert?
No listing for Guanxian Ruichang Trading 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 Guanxian Ruichang Trading Co., Ltd?
Yes. FDA refused 1 shipment line from Guanxian Ruichang Trading Co., Ltd on January 11, 2022. The most recent, on January 11, 2022, was wheat gluten, charged as MELAMINE (melamine).
Why did FDA refuse Guanxian Ruichang Trading Co., Ltd's shipments?
The most frequent charge is MELAMINE (melamine, 1 line).
What is Guanxian Ruichang Trading Co., Ltd's FEI number?
Guanxian Ruichang Trading Co., Ltd's FDA Establishment Identifier (FEI) is 3010406060.

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Example subjectGuanxian Ruichang Trading Co., 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.