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PT. Citra Deli Kreasitama

FDA import alert and refusal historyJakarta Utara, IndonesiaFEI 3004390932

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Example subjectPT. Citra Deli Kreasitam added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Citra Deli Kreasitama (Jakarta Utara, Indonesia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for sari temulawak drink mix, published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for PT. Citra Deli Kreasitama

1 record, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listSari Temulawak Drink Mix
    Source

Questions about PT. Citra Deli Kreasitama

Is PT. Citra Deli Kreasitama on an FDA import alert?
Yes. As of October 26, 2026, PT. Citra Deli Kreasitama is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sari temulawak drink mix; FDA published the listing on September 18, 2009.
Has FDA refused shipments from PT. Citra Deli Kreasitama?
No FDA import refusals for PT. Citra Deli Kreasitama appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is PT. Citra Deli Kreasitama's FEI number?
PT. Citra Deli Kreasitama's FDA Establishment Identifier (FEI) is 3004390932.
Can shipments from PT. Citra Deli Kreasitama still enter the U.S.?
Shipments of sari temulawak drink mix from PT. Citra Deli Kreasitama can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).

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Example subjectPT. Citra Deli Kreasitam 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.