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PT Dempo Andalas Samudera

FDA import alert and refusal historyPadang, IndonesiaFEI 3006430536

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Example subjectPT Dempo Andalas Samuder added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT Dempo Andalas Samudera has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 21, 2019, 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 Dempo Andalas Samudera

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

2019

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

2014

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

Questions about PT Dempo Andalas Samudera

Is PT Dempo Andalas Samudera on an FDA import alert?
No listing for PT Dempo Andalas Samudera 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 Dempo Andalas Samudera?
No FDA import refusals for PT Dempo Andalas Samudera appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was PT Dempo Andalas Samudera last inspected by FDA?
FDA's most recent inspection of PT Dempo Andalas Samudera with a final classification is dated June 21, 2019 and was classified VAI (Voluntary Action Indicated).
What is PT Dempo Andalas Samudera's FEI number?
PT Dempo Andalas Samudera's FDA Establishment Identifier (FEI) is 3006430536.

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Example subjectPT Dempo Andalas Samuder 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.