Tunggal Jaya Prima
FDA import alert and refusal historyDeli Serdang, IndonesiaFEI 3004260043
As of October 26, 2026, Tunggal Jaya Prima (Deli Serdang, Indonesia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for passion fruit, topping or syrup; subtropical and tropical fruit, topping or syrup, n.e.c.; syrups and molasses, n.e.c.; eggplant syrup, 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
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Tunggal Jaya Prima
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listPassion Fruit, Topping or Syrup; Subtropical and Tropical Fruit, Topping or Syrup, N.E.C.; Syrups and Molasses, N.E.C.; eggplant syrupSource
Questions about Tunggal Jaya Prima
- Is Tunggal Jaya Prima on an FDA import alert?
- Yes. As of October 26, 2026, Tunggal Jaya Prima is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for passion fruit, topping or syrup; subtropical and tropical fruit, topping or syrup, n.e.c.; syrups and molasses, n.e.c.; eggplant syrup; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Tunggal Jaya Prima?
- No FDA import refusals for Tunggal Jaya Prima appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Tunggal Jaya Prima's FEI number?
- Tunggal Jaya Prima's FDA Establishment Identifier (FEI) is 3004260043.
- Can shipments from Tunggal Jaya Prima still enter the U.S.?
- Shipments of passion fruit, topping or syrup; subtropical and tropical fruit, topping or syrup, n.e.c.; syrups and molasses, n.e.c.; eggplant syrup from Tunggal Jaya Prima 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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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.