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PT. Halimas Mina Utama

FDA import alert and refusal historyJakarta, IndonesiaFEI 3004250044

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Example subjectPT. Halimas Mina Utam added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Halimas Mina Utama (Jakarta, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for frog legs, published by FDA on April 10, 2025, is also listed on Import Alert 16-18 (green 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. Halimas Mina Utama

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

2025

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

2009

  1. Import alert listing
    Listed on Import Alert 16-18green listRaw Shrimp
    Source

Questions about PT. Halimas Mina Utama

Is PT. Halimas Mina Utama on an FDA import alert?
Yes. As of October 26, 2026, PT. Halimas Mina Utama is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for frog legs; FDA published the listing on April 10, 2025.
Has FDA refused shipments from PT. Halimas Mina Utama?
No FDA import refusals for PT. Halimas Mina Utama appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is PT. Halimas Mina Utama's FEI number?
PT. Halimas Mina Utama's FDA Establishment Identifier (FEI) is 3004250044.
Can shipments from PT. Halimas Mina Utama still enter the U.S.?
Shipments of frog legs from PT. Halimas Mina Utama 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 subjectPT. Halimas Mina Utam 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.