SupplierRadar

Pt. Pasura Koerinci

FDA import alert and refusal historyPadang, IndonesiaFEI 3012119989

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Example subjectPt. Pasura Koerinc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Pt. Pasura Koerinci has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 21, 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. Pasura Koerinci

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

2012

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Food and Color Additives Petition Review; Foodborne Biological Hazards; Pesticides and Chemical Contaminants
    Source

Questions about Pt. Pasura Koerinci

Is Pt. Pasura Koerinci on an FDA import alert?
No listing for Pt. Pasura Koerinci 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. Pasura Koerinci?
No FDA import refusals for Pt. Pasura Koerinci appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Pt. Pasura Koerinci last inspected by FDA?
FDA's most recent inspection of Pt. Pasura Koerinci with a final classification is dated September 21, 2018 and was classified VAI (Voluntary Action Indicated).
What is Pt. Pasura Koerinci's FEI number?
Pt. Pasura Koerinci's FDA Establishment Identifier (FEI) is 3012119989.

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Example subjectPt. Pasura Koerinc 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.