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PT. Lautan Murti

FDA import alert and refusal historyCilacap, IndonesiaFEI 3004331782

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Example subjectPT. Lautan Murt added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Lautan Murti (Cilacap, Indonesia) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for tuna (albacore, yellowfin, bluefin, skipjack, etc.), published by FDA on September 10, 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 PT. Lautan Murti

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

2009

  1. Import alert listing
    Listed on Import Alert 16-105red listTuna (Albacore, Yellowfin, Bluefin, Skipjack, Etc.)
    Source

Questions about PT. Lautan Murti

Is PT. Lautan Murti on an FDA import alert?
Yes. As of October 26, 2026, PT. Lautan Murti is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for tuna (albacore, yellowfin, bluefin, skipjack, etc.); FDA published the listing on September 10, 2009.
Has FDA refused shipments from PT. Lautan Murti?
No FDA import refusals for PT. Lautan Murti appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is PT. Lautan Murti's FEI number?
PT. Lautan Murti's FDA Establishment Identifier (FEI) is 3004331782.
Can shipments from PT. Lautan Murti still enter the U.S.?
Shipments of tuna (albacore, yellowfin, bluefin, skipjack, etc.) from PT. Lautan Murti 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 subjectPT. Lautan Murt 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.