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PT Wirontono Baru

FDA import alert and refusal historyJakarta, IndonesiaFEI 3013264783

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Example subjectPT Wirontono Bar added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT Wirontono Baru is on the green list of FDA Import Alert 16-18, which exempts its listed products from detention without physical examination under that alert, and has 1 FDA import refusal recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
Shrimp & prawns · LISTERIA
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for PT Wirontono Baru

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

2023

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2021

  1. Import refusal
    Refused, Shrimp & prawnsLISTERIAEntry 98K-2229210-8
    Source

2018

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2010

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

Refusal charges, in plain English

  • LISTERIA1 refused line

    Listeria monocytogenes

    The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about PT Wirontono Baru

Is PT Wirontono Baru on an FDA import alert?
Yes. As of October 26, 2026, PT Wirontono Baru is on the green list of FDA Import Alert 16-18, “Raw shrimp”, for raw shrimp; FDA published the listing on December 14, 2010.
Has FDA refused shipments from PT Wirontono Baru?
Yes. FDA refused 1 shipment line from PT Wirontono Baru on December 20, 2021. The most recent, on December 20, 2021, was shrimp & prawns, charged as LISTERIA (listeria monocytogenes).
Why did FDA refuse PT Wirontono Baru's shipments?
The most frequent charge is LISTERIA (listeria monocytogenes, 1 line).
When was PT Wirontono Baru last inspected by FDA?
FDA's most recent inspection of PT Wirontono Baru with a final classification is dated May 10, 2023 and was classified VAI (Voluntary Action Indicated).
What is PT Wirontono Baru's FEI number?
PT Wirontono Baru's FDA Establishment Identifier (FEI) is 3013264783.

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Example subjectPT Wirontono Bar 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.