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Gallant Ocean International, Inc. Xiaogang Plant

FDA import alert and refusal historyKaohsiung, TaiwanFEI 3006313857

Recorded by FDA as GALLANT OCEAN INTERNATIONAL, INC. XIAOGANG PLANT

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Example subjectGallant Ocean International, Inc. Xiaogang Plan added to Import Alert 16-129 (red list)

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As of October 26, 2026, Gallant Ocean International, Inc. Xiaogang Plant (KAOHSIUNG, Taiwan) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for barramundi; lates calcarifer; koral; asian seabass, published by FDA on May 19, 2023, and has 8 FDA import refusals recorded since October 2016.

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

Current status

Import alerts
IA 16-81 · red list
Last import refusal
Barramundi · SALMONELLA
Last warning letter
None found
Last inspection
None on record

Every FDA record for Gallant Ocean International, Inc. Xiaogang Plant

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

2025

  1. Import refusal
    Refused, BarramundiSALMONELLAEntry GL5-5444478-3
    Source

2023

  1. Import refusal
    Refused, 2 lines in one entry: BarramundiSALMONELLAEntry AQZ-0558840-8Show 2 lines
    Source
  2. Import refusal
    Refused, BarramundiSALMONELLAEntry KM6-3596453-9
    Source
  3. Import alert listing
    Listed on Import Alert 16-81red listBarramundi; Lates calcarifer; Koral; Asian Seabass
    Source

2021

  1. Import refusal
    Refused, 2 lines in one entry: Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry GL5-5282128-9Show 2 lines
    • Refused, Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry GL5-5282128-9Source
    • Refused, Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry GL5-5282128-9Source
    Source

2019

  1. Import refusal
    Refused, TilapiaSALMONELLAEntry EBH-0083281-9
    Source

2017

  1. Import refusal
    Refused, Tilapia, aquaculture harvested fishery/seafood productsSALMONELLAEntry KM6-3509366-9
    Source

Refusal charges, in plain English

  • SALMONELLA6 refused lines

    Salmonella

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

  • VETDRUGRES2 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.

Questions about Gallant Ocean International, Inc. Xiaogang Plant

Is Gallant Ocean International, Inc. Xiaogang Plant on an FDA import alert?
Yes. As of October 26, 2026, Gallant Ocean International, Inc. Xiaogang Plant is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for barramundi; lates calcarifer; koral; asian seabass; FDA published the listing on May 19, 2023.
Has FDA refused shipments from Gallant Ocean International, Inc. Xiaogang Plant?
Yes. FDA refused 8 shipment lines from Gallant Ocean International, Inc. Xiaogang Plant between December 5, 2017 and November 25, 2025. The most recent, on November 25, 2025, was barramundi, charged as SALMONELLA (salmonella).
Why did FDA refuse Gallant Ocean International, Inc. Xiaogang Plant's shipments?
The most frequent charges are SALMONELLA (salmonella, 6 lines) and VETDRUGRES (animal drug residue, 2 lines).
What is Gallant Ocean International, Inc. Xiaogang Plant's FEI number?
Gallant Ocean International, Inc. Xiaogang Plant's FDA Establishment Identifier (FEI) is 3006313857.
Can shipments from Gallant Ocean International, Inc. Xiaogang Plant still enter the U.S.?
Shipments of barramundi; lates calcarifer; koral; asian seabass from Gallant Ocean International, Inc. Xiaogang Plant can be detained without physical examination under Import Alert 16-81; 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 subjectGallant Ocean International, Inc. Xiaogang Plan 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.