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PT. Enam Delapan Sembilan

FDA import alert and refusal historyLamongan, IndonesiaFEI 3006441841

Recorded by FDA as PT. ENAM DELAPAN SEMBILAN

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Example subjectPT. Enam Delapan Sembila added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Enam Delapan Sembilan (Lamongan, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for scarlet snapper; tilapia, published by FDA on November 16, 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 PT. Enam Delapan Sembilan

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

2010

  1. Import alert listing
    Listed on Import Alert 16-81red listScarlet Snapper; Tilapia
    Source

Questions about PT. Enam Delapan Sembilan

Is PT. Enam Delapan Sembilan on an FDA import alert?
Yes. As of October 26, 2026, PT. Enam Delapan Sembilan is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for scarlet snapper; tilapia; FDA published the listing on November 16, 2010.
Has FDA refused shipments from PT. Enam Delapan Sembilan?
No FDA import refusals for PT. Enam Delapan Sembilan appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is PT. Enam Delapan Sembilan's FEI number?
PT. Enam Delapan Sembilan's FDA Establishment Identifier (FEI) is 3006441841.
Can shipments from PT. Enam Delapan Sembilan still enter the U.S.?
Shipments of scarlet snapper; tilapia from PT. Enam Delapan Sembilan 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. Enam Delapan Sembila 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.