SupplierRadar

PT Juifa International Foods

FDA import alert and refusal historyCilacep, IndonesiaFEI 3002986890

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Example subjectPT Juifa International Food added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT Juifa International Foods has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 19, 2018, 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 Juifa International Foods

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

2018

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2012

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

Questions about PT Juifa International Foods

Is PT Juifa International Foods on an FDA import alert?
No listing for PT Juifa International Foods 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 Juifa International Foods?
No FDA import refusals for PT Juifa International Foods appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was PT Juifa International Foods last inspected by FDA?
FDA's most recent inspection of PT Juifa International Foods with a final classification is dated January 19, 2018 and was classified NAI (No Action Indicated).
What is PT Juifa International Foods's FEI number?
PT Juifa International Foods's FDA Establishment Identifier (FEI) is 3002986890.

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Example subjectPT Juifa International Food 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.