Worldgate Vision Beverage Sdn Bhd
FDA import alert and refusal historyKuala Muda, MalaysiaFEI 3011235150
As of October 26, 2026, Worldgate Vision Beverage Sdn Bhd (Kuala Muda, Malaysia) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for kopi jantan tradisional natural herbs coffee; natural herbs coffee; stiff bull herbal coffee, published by FDA on August 5, 2016, 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 54-16 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Worldgate Vision Beverage Sdn Bhd
1 record, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 54-16red listKopi Jantan Tradisional Natural Herbs Coffee; Natural Herbs Coffee; STIFF BULL HERBAL COFFEESource
Questions about Worldgate Vision Beverage Sdn Bhd
- Is Worldgate Vision Beverage Sdn Bhd on an FDA import alert?
- Yes. As of October 26, 2026, Worldgate Vision Beverage Sdn Bhd is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for kopi jantan tradisional natural herbs coffee; natural herbs coffee; stiff bull herbal coffee; FDA published the listing on August 5, 2016.
- Has FDA refused shipments from Worldgate Vision Beverage Sdn Bhd?
- No FDA import refusals for Worldgate Vision Beverage Sdn Bhd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Worldgate Vision Beverage Sdn Bhd's FEI number?
- Worldgate Vision Beverage Sdn Bhd's FDA Establishment Identifier (FEI) is 3011235150.
- Can shipments from Worldgate Vision Beverage Sdn Bhd still enter the U.S.?
- Shipments of kopi jantan tradisional natural herbs coffee; natural herbs coffee; stiff bull herbal coffee from Worldgate Vision Beverage Sdn Bhd can be detained without physical examination under Import Alert 54-16; 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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