SupplierRadar

PT Pan Putra Samudra

FDA import alert and refusal historyRembang, IndonesiaFEI 3010784610

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Example subjectPT Pan Putra Samudr added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT Pan Putra Samudra has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on February 1, 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 Pan Putra Samudra

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

2015

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

Questions about PT Pan Putra Samudra

Is PT Pan Putra Samudra on an FDA import alert?
No listing for PT Pan Putra Samudra 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 Pan Putra Samudra?
No FDA import refusals for PT Pan Putra Samudra appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was PT Pan Putra Samudra last inspected by FDA?
FDA's most recent inspection of PT Pan Putra Samudra with a final classification is dated February 1, 2019 and was classified VAI (Voluntary Action Indicated).
What is PT Pan Putra Samudra's FEI number?
PT Pan Putra Samudra's FDA Establishment Identifier (FEI) is 3010784610.

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Example subjectPT Pan Putra Samudr 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.