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Zhanjiang Longwei Aquatic Products Industry Co., Ltd.

FDA import alert and refusal historyZhanjiang, ChinaFEI 2000041911

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Example subjectZhanjiang Longwei Aquatic Products Industry Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Zhanjiang Longwei Aquatic Products Industry Co., Ltd. is on the green list of FDA Import Alert 16-131, which exempts its listed products from detention without physical examination under that alert, and has 10 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Shrimp & prawns, breaded · VETDRUGRES
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Zhanjiang Longwei Aquatic Products Industry Co., Ltd.

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

2020

  1. Import alert listing
    Listed on Import Alert 16-131green listShrimp
    Source

2019

  1. Import refusal
    Refused, 2 lines in one entry: Shrimp & prawns, breadedVETDRUGRESEntry 595-5580417-4Show 2 lines
    Source

2018

  1. Import refusal
    Refused, Shrimp & prawns, breadedUNSAFE ADDVETDRUGRESEntry 595-5558316-6
    Source
  2. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsUNSAFE ADDVETDRUGRESEntry D52-0023429-7
    Source
  3. Import refusal
    Refused, Shrimp & prawns, breadedUNSAFE ADDVETDRUGRESEntry 595-5558316-6
    Source
  4. Import refusal
    Refused, 2 lines in one entry: Shrimp & prawns, breadedVETDRUGRESEntry BEZ-0008431-7Show 2 lines
    Source
  5. Import refusal
    Refused, 3 lines in one entry: Shrimp & prawns, breadedNITROFURANEntry BEZ-0007870-7Show 3 lines
    Source

2013

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • VETDRUGRES7 refused lines

    Animal drug residue

    The product appeared to contain a new animal drug, or a conversion product of one, that is unsafe within the meaning of section 512 of the FD&C Act.

  • NITROFURAN3 refused lines

    Nitrofurans

    The product appeared to contain nitrofurans, a class of antibiotic drugs, which are treated as an unsafe food additive under section 409 of the FD&C Act.

  • UNSAFE ADD3 refused lines

    Food additive unsafe under section 409

    The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

Questions about Zhanjiang Longwei Aquatic Products Industry Co., Ltd.

Is Zhanjiang Longwei Aquatic Products Industry Co., Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Zhanjiang Longwei Aquatic Products Industry Co., Ltd. is on the green list of FDA Import Alert 16-131, “Aquacultured, Shrimp, Dace, and Eel from China and Hong…”, for shrimp; FDA published the listing on June 5, 2020.
Has FDA refused shipments from Zhanjiang Longwei Aquatic Products Industry Co., Ltd.?
Yes. FDA refused 10 shipment lines from Zhanjiang Longwei Aquatic Products Industry Co., Ltd. between March 19, 2018 and July 10, 2019. The most recent, on July 10, 2019, was shrimp & prawns, breaded, charged as VETDRUGRES (animal drug residue).
Why did FDA refuse Zhanjiang Longwei Aquatic Products Industry Co., Ltd.'s shipments?
The most frequent charges are VETDRUGRES (animal drug residue, 7 lines) and NITROFURAN (nitrofurans, 3 lines).
When was Zhanjiang Longwei Aquatic Products Industry Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Zhanjiang Longwei Aquatic Products Industry Co., Ltd. with a final classification is dated May 10, 2013 and was classified NAI (No Action Indicated).
What is Zhanjiang Longwei Aquatic Products Industry Co., Ltd.'s FEI number?
Zhanjiang Longwei Aquatic Products Industry Co., Ltd.'s FDA Establishment Identifier (FEI) is 2000041911.

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Example subjectZhanjiang Longwei Aquatic Products Industry Co., Ltd 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.