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PT Ujung Timur Sidoarjo

FDA import alert and refusal historySidoarjo, IndonesiaFEI 3008140352

Recorded by FDA as PT UJUNG TIMUR SIDOARJO

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Example subjectPT Ujung Timur Sidoarj added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT Ujung Timur Sidoarjo (Sidoarjo, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for snapper (red, gray, malabar, etc.), published by FDA on September 18, 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 Ujung Timur Sidoarjo

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

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listSnapper (Red, Gray, Malabar, etc.)
    Source

Questions about PT Ujung Timur Sidoarjo

Is PT Ujung Timur Sidoarjo on an FDA import alert?
Yes. As of October 26, 2026, PT Ujung Timur Sidoarjo is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for snapper (red, gray, malabar, etc.); FDA published the listing on September 18, 2009.
Has FDA refused shipments from PT Ujung Timur Sidoarjo?
No FDA import refusals for PT Ujung Timur Sidoarjo appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is PT Ujung Timur Sidoarjo's FEI number?
PT Ujung Timur Sidoarjo's FDA Establishment Identifier (FEI) is 3008140352.
Can shipments from PT Ujung Timur Sidoarjo still enter the U.S.?
Shipments of snapper (red, gray, malabar, etc.) from PT Ujung Timur Sidoarjo 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 Ujung Timur Sidoarj 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.