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PT. Ayu Bumi Sejati

FDA import alert and refusal historyMedan, IndonesiaFEI 3004250678

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Example subjectPT. Ayu Bumi Sejat added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Ayu Bumi Sejati 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 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
Classified VAI (Voluntary Action Indicated)

Every FDA record for PT. Ayu Bumi Sejati

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

2018

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

2015

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source
  2. Import alert listing
    Listed on Import Alert 16-18green listRaw Shrimp
    Source

Questions about PT. Ayu Bumi Sejati

Is PT. Ayu Bumi Sejati on an FDA import alert?
Yes. As of October 26, 2026, PT. Ayu Bumi Sejati is on the green list of FDA Import Alert 16-18, “Raw shrimp”, for raw shrimp; FDA published the listing on April 3, 2015.
Has FDA refused shipments from PT. Ayu Bumi Sejati?
No FDA import refusals for PT. Ayu Bumi Sejati appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was PT. Ayu Bumi Sejati last inspected by FDA?
FDA's most recent inspection of PT. Ayu Bumi Sejati with a final classification is dated September 14, 2018 and was classified VAI (Voluntary Action Indicated).
What is PT. Ayu Bumi Sejati's FEI number?
PT. Ayu Bumi Sejati's FDA Establishment Identifier (FEI) is 3004250678.

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Example subjectPT. Ayu Bumi Sejat 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.