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Yongfatt Vision Tr

FDA import alert and refusal historySungai Petani, MalaysiaFEI 3012104071

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Example subjectYongfatt Vision T added to Import Alert 16-129 (red list)

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As of October 25, 2026, Yongfatt Vision Tr (Sungai Petani, 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, published by FDA on September 19, 2017, 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 Yongfatt Vision Tr

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

2017

  1. Import alert listing
    Listed on Import Alert 54-16red listKopi Jantan Tradisional Natural Herbs Coffee
    Source

Questions about Yongfatt Vision Tr

Is Yongfatt Vision Tr on an FDA import alert?
Yes. As of October 25, 2026, Yongfatt Vision Tr is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for kopi jantan tradisional natural herbs coffee; FDA published the listing on September 19, 2017.
Has FDA refused shipments from Yongfatt Vision Tr?
No FDA import refusals for Yongfatt Vision Tr appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Yongfatt Vision Tr's FEI number?
Yongfatt Vision Tr's FDA Establishment Identifier (FEI) is 3012104071.
Can shipments from Yongfatt Vision Tr still enter the U.S.?
Shipments of kopi jantan tradisional natural herbs coffee from Yongfatt Vision Tr 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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Example subjectYongfatt Vision T 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.