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Giang Ky Co Ltd.

FDA import alert and refusal historyHo Chi Minh City, VietnamFEI 3003002783

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Example subjectGiang Ky Co Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Giang Ky Co Ltd. (Ho Chi Minh City, Vietnam) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for dried sweet rice; shredded tapioca; dried gooseberry, 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 Giang Ky 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 45-02red listdried sweet rice; shredded tapioca; dried gooseberry
    Source

Questions about Giang Ky Co Ltd.

Is Giang Ky Co Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Giang Ky Co Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for dried sweet rice; shredded tapioca; dried gooseberry; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Giang Ky Co Ltd.?
No FDA import refusals for Giang Ky Co Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Giang Ky Co Ltd.'s FEI number?
Giang Ky Co Ltd.'s FDA Establishment Identifier (FEI) is 3003002783.
Can shipments from Giang Ky Co Ltd. still enter the U.S.?
Shipments of dried sweet rice; shredded tapioca; dried gooseberry from Giang Ky Co Ltd. can be detained without physical examination under Import Alert 45-02; 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 subjectGiang Ky 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.