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Goldenfish TA Co, Ltd

FDA import alert and refusal historyHochiminh City, VietnamFEI 2000033262

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Example subjectGoldenfish TA Co, Lt added to Import Alert 16-129 (red list)

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As of October 26, 2026, Goldenfish TA Co, Ltd (Hochiminh City, Vietnam) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for frog legs; snails, aquatic, other aquatic species, published by FDA on September 18, 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 Goldenfish TA Co, Ltd

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

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listFrog Legs; Snails, Aquatic, Other Aquatic Species
    Source

Questions about Goldenfish TA Co, Ltd

Is Goldenfish TA Co, Ltd on an FDA import alert?
Yes. As of October 26, 2026, Goldenfish TA Co, Ltd is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for frog legs; snails, aquatic, other aquatic species; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Goldenfish TA Co, Ltd?
No FDA import refusals for Goldenfish TA Co, Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Goldenfish TA Co, Ltd's FEI number?
Goldenfish TA Co, Ltd's FDA Establishment Identifier (FEI) is 2000033262.
Can shipments from Goldenfish TA Co, Ltd still enter the U.S.?
Shipments of frog legs; snails, aquatic, other aquatic species from Goldenfish TA Co, Ltd 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 subjectGoldenfish TA 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.