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Hoom Xiang Industries Sdn. Bhd.

FDA import alert and refusal historyBukit Mertajam, MalaysiaFEI 3004343595

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Example subjectHoom Xiang Industries Sdn. Bhd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Hoom Xiang Industries Sdn. Bhd. (Bukit Mertajam, Malaysia) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for tuna, published by FDA on November 24, 2010, 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 Hoom Xiang Industries Sdn. Bhd.

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

2010

  1. Import alert listing
    Listed on Import Alert 16-105red listTuna
    Source

Questions about Hoom Xiang Industries Sdn. Bhd.

Is Hoom Xiang Industries Sdn. Bhd. on an FDA import alert?
Yes. As of October 26, 2026, Hoom Xiang Industries Sdn. Bhd. is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for tuna; FDA published the listing on November 24, 2010.
Has FDA refused shipments from Hoom Xiang Industries Sdn. Bhd.?
No FDA import refusals for Hoom Xiang Industries Sdn. Bhd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Hoom Xiang Industries Sdn. Bhd.'s FEI number?
Hoom Xiang Industries Sdn. Bhd.'s FDA Establishment Identifier (FEI) is 3004343595.
Can shipments from Hoom Xiang Industries Sdn. Bhd. still enter the U.S.?
Shipments of tuna from Hoom Xiang Industries Sdn. Bhd. can be detained without physical examination under Import Alert 16-105; 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 subjectHoom Xiang Industries Sdn. Bhd 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.