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PT. Serena Indopangan Industri

FDA import alert and refusal historyCibinong, IndonesiaFEI 3008847216

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Example subjectPT. Serena Indopangan Industr added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Serena Indopangan Industri has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on October 16, 2018, was classified VAI (Voluntary Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for PT. Serena Indopangan Industri

2 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)Foodborne Biological Hazards
    Source

Questions about PT. Serena Indopangan Industri

Is PT. Serena Indopangan Industri on an FDA import alert?
No listing for PT. Serena Indopangan Industri appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
Has FDA refused shipments from PT. Serena Indopangan Industri?
No FDA import refusals for PT. Serena Indopangan Industri appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was PT. Serena Indopangan Industri last inspected by FDA?
FDA's most recent inspection of PT. Serena Indopangan Industri with a final classification is dated October 16, 2018 and was classified VAI (Voluntary Action Indicated).
What is PT. Serena Indopangan Industri's FEI number?
PT. Serena Indopangan Industri's FDA Establishment Identifier (FEI) is 3008847216.

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Example subjectPT. Serena Indopangan Industr 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.