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Xiamen Liangfa Imp & Exp Trade Co.

FDA import alert and refusal historyXiamen, ChinaFEI 3003259459

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Example subjectXiamen Liangfa Imp & Exp Trade Co added to Import Alert 16-129 (red list)

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As of October 26, 2026, Xiamen Liangfa Imp & Exp Trade Co. (Xiamen, China) is on the red list of FDA Import Alert 16-127 (Seafood: chloramphenicol) for crab, published by FDA on September 16, 2009, and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Xiamen Liangfa Imp & Exp Trade Co.

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

2009

  1. Import alert listing
    Listed on Import Alert 16-127red listCrab
    Source

Questions about Xiamen Liangfa Imp & Exp Trade Co.

Is Xiamen Liangfa Imp & Exp Trade Co. on an FDA import alert?
Yes. As of October 26, 2026, Xiamen Liangfa Imp & Exp Trade Co. is on the red list of FDA Import Alert 16-127, “Seafood: chloramphenicol”, for crab; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Xiamen Liangfa Imp & Exp Trade Co.?
No FDA import refusals for Xiamen Liangfa Imp & Exp Trade Co. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Xiamen Liangfa Imp & Exp Trade Co.'s FEI number?
Xiamen Liangfa Imp & Exp Trade Co.'s FDA Establishment Identifier (FEI) is 3003259459.
Can shipments from Xiamen Liangfa Imp & Exp Trade Co. still enter the U.S.?
Shipments of crab from Xiamen Liangfa Imp & Exp Trade Co. can be detained without physical examination under Import Alert 16-127; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectXiamen Liangfa Imp & Exp Trade Co 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.