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Beihai Evergreen Aquatic Product Science&Technology Co., LTD

FDA import alert and refusal historyBeihai, ChinaFEI 3007515837

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Example subjectBeihai Evergreen Aquatic Product Science&Technology Co., LT added to Import Alert 16-129 (red list)

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As of October 27, 2026, Beihai Evergreen Aquatic Product Science&Technology Co., LTD (Beihai, China) is on the red list of FDA Import Alert 16-124 (Aquaculture seafood: unapproved drugs) for pompano, published by FDA on April 24, 2024, is also listed on Import Alert 16-81 (red list), and has 2 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Pompano (permit, pompanito) · VETDRUGRES
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Beihai Evergreen Aquatic Product Science&Technology Co., LTD

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

2024

  1. Import alert listing
    Listed on Import Alert 16-124red listPompano
    Source
  2. Import refusal
    Refused, Pompano (permit, pompanito)VETDRUGRESEntry BDD-0834014-9
    Source

2019

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

2018

  1. Import alert listing
    Listed on Import Alert 16-81red listFrozen Tilapia Fish Whole
    Source
  2. Import refusal
    Refused, Tilapia, aquaculture harvested fishery/seafood productsSALMONELLAEntry 417-0324296-0
    Source

2017

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • SALMONELLA1 refused line

    Salmonella

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

  • VETDRUGRES1 refused line

    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.

Questions about Beihai Evergreen Aquatic Product Science&Technology Co., LTD

Is Beihai Evergreen Aquatic Product Science&Technology Co., LTD on an FDA import alert?
Yes. As of October 27, 2026, Beihai Evergreen Aquatic Product Science&Technology Co., LTD is on the red list of FDA Import Alert 16-124, “Aquaculture seafood: unapproved drugs”, for pompano; FDA published the listing on April 24, 2024.
Has FDA refused shipments from Beihai Evergreen Aquatic Product Science&Technology Co., LTD?
Yes. FDA refused 2 shipment lines from Beihai Evergreen Aquatic Product Science&Technology Co., LTD between February 1, 2018 and March 13, 2024. The most recent, on March 13, 2024, was pompano (permit, pompanito), charged as VETDRUGRES (animal drug residue).
Why did FDA refuse Beihai Evergreen Aquatic Product Science&Technology Co., LTD's shipments?
The most frequent charges are SALMONELLA (salmonella, 1 line) and VETDRUGRES (animal drug residue, 1 line).
When was Beihai Evergreen Aquatic Product Science&Technology Co., LTD last inspected by FDA?
FDA's most recent inspection of Beihai Evergreen Aquatic Product Science&Technology Co., LTD with a final classification is dated September 4, 2019 and was classified NAI (No Action Indicated).
What is Beihai Evergreen Aquatic Product Science&Technology Co., LTD's FEI number?
Beihai Evergreen Aquatic Product Science&Technology Co., LTD's FDA Establishment Identifier (FEI) is 3007515837.
Can shipments from Beihai Evergreen Aquatic Product Science&Technology Co., LTD still enter the U.S.?
Shipments of pompano from Beihai Evergreen Aquatic Product Science&Technology Co., LTD can be detained without physical examination under Import Alert 16-124; 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 subjectBeihai Evergreen Aquatic Product Science&Technology 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.