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PT. Sarimakmur Tunggal Mandiri

FDA import alert and refusal historyMedan, IndonesiaFEI 3008638136

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Example subjectPT. Sarimakmur Tunggal Mandir added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Sarimakmur Tunggal Mandiri has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on June 1, 2016, was classified NAI (No 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 NAI (No Action Indicated)

Every FDA record for PT. Sarimakmur Tunggal Mandiri

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

2016

  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

Questions about PT. Sarimakmur Tunggal Mandiri

Is PT. Sarimakmur Tunggal Mandiri on an FDA import alert?
No listing for PT. Sarimakmur Tunggal Mandiri 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. Sarimakmur Tunggal Mandiri?
No FDA import refusals for PT. Sarimakmur Tunggal Mandiri appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was PT. Sarimakmur Tunggal Mandiri last inspected by FDA?
FDA's most recent inspection of PT. Sarimakmur Tunggal Mandiri with a final classification is dated June 1, 2016 and was classified NAI (No Action Indicated).
What is PT. Sarimakmur Tunggal Mandiri's FEI number?
PT. Sarimakmur Tunggal Mandiri's FDA Establishment Identifier (FEI) is 3008638136.

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Example subjectPT. Sarimakmur Tunggal Mandir 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.