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PT. Galaxi Nusa Dua

FDA import alert and refusal historyBekasi, IndonesiaFEI 3010716890

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Example subjectPT. Galaxi Nusa Du added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Galaxi Nusa Dua (Bekasi, Indonesia) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for frozen tuna, published by FDA on March 20, 2018, is also listed on Import Alert 16-81 (red list), 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 PT. Galaxi Nusa Dua

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

2018

  1. Import alert listing
    Listed on Import Alert 16-120red listFrozen Tuna
    Source

2017

  1. Import alert listing
    Listed on Import Alert 16-81red listTuna
    Source

Questions about PT. Galaxi Nusa Dua

Is PT. Galaxi Nusa Dua on an FDA import alert?
Yes. As of October 26, 2026, PT. Galaxi Nusa Dua is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for frozen tuna; FDA published the listing on March 20, 2018.
Has FDA refused shipments from PT. Galaxi Nusa Dua?
No FDA import refusals for PT. Galaxi Nusa Dua appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is PT. Galaxi Nusa Dua's FEI number?
PT. Galaxi Nusa Dua's FDA Establishment Identifier (FEI) is 3010716890.
Can shipments from PT. Galaxi Nusa Dua still enter the U.S.?
Shipments of frozen tuna from PT. Galaxi Nusa Dua can be detained without physical examination under Import Alert 16-120; 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 subjectPT. Galaxi Nusa Du 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.