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PT Bumi Menara Internusa - Dampit

FDA import alert and refusal historyDampit, Malang, IndonesiaFEI 3003203635

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Example subjectPT Bumi Menara Internusa - Dampi added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT Bumi Menara Internusa - Dampit 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 8 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · FILTHY
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for PT Bumi Menara Internusa - Dampit

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

2022

  1. Import refusal
    Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0755200-9Show 3 lines
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0755200-9Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0755200-9Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0755200-9Source
    Source
  2. Import refusal
    Refused, 5 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 594-0342446-4Show 5 lines
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 594-0342446-4Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 594-0342446-4Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 594-0342446-4Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 594-0342446-4Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 594-0342446-4Source
    Source

2018

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2012

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

2009

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

Refusal charges, in plain English

  • SALMONELLA5 refused lines

    Salmonella

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

  • FILTHY3 refused lines

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about PT Bumi Menara Internusa - Dampit

Is PT Bumi Menara Internusa - Dampit on an FDA import alert?
Yes. As of October 26, 2026, PT Bumi Menara Internusa - Dampit is on the green list of FDA Import Alert 16-18, “Raw shrimp”, for raw shrimp; FDA published the listing on November 24, 2009.
Has FDA refused shipments from PT Bumi Menara Internusa - Dampit?
Yes. FDA refused 8 shipment lines from PT Bumi Menara Internusa - Dampit between June 1, 2022 and June 23, 2022. The most recent, on June 23, 2022, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse PT Bumi Menara Internusa - Dampit's shipments?
The most frequent charges are SALMONELLA (salmonella, 5 lines) and FILTHY (filthy, putrid or decomposed substance, 3 lines).
When was PT Bumi Menara Internusa - Dampit last inspected by FDA?
FDA's most recent inspection of PT Bumi Menara Internusa - Dampit with a final classification is dated January 16, 2018 and was classified NAI (No Action Indicated).
What is PT Bumi Menara Internusa - Dampit's FEI number?
PT Bumi Menara Internusa - Dampit's FDA Establishment Identifier (FEI) is 3003203635.

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Example subjectPT Bumi Menara Internusa - Dampi 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.