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Jaymen Mack Enterprise

FDA import alert and refusal historyBukit Mertajam, MalaysiaFEI 3008381023

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Example subjectJaymen Mack Enterpris added to Import Alert 16-129 (red list)

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As of October 26, 2026, Jaymen Mack Enterprise (Bukit Mertajam, Malaysia) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for uncaria gembier; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii), published by FDA on February 28, 2014, 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 Jaymen Mack Enterprise

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

2014

  1. Import alert listing
    Listed on Import Alert 54-15red listUncaria Gembier; Kratom (Herbal and Botanical Teas II, continued); Kratom (Herbal and Botanicals, not Teas II)
    Source

Questions about Jaymen Mack Enterprise

Is Jaymen Mack Enterprise on an FDA import alert?
Yes. As of October 26, 2026, Jaymen Mack Enterprise is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for uncaria gembier; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); FDA published the listing on February 28, 2014.
Has FDA refused shipments from Jaymen Mack Enterprise?
No FDA import refusals for Jaymen Mack Enterprise appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Jaymen Mack Enterprise's FEI number?
Jaymen Mack Enterprise's FDA Establishment Identifier (FEI) is 3008381023.
Can shipments from Jaymen Mack Enterprise still enter the U.S.?
Shipments of uncaria gembier; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii) from Jaymen Mack Enterprise can be detained without physical examination under Import Alert 54-15; 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 subjectJaymen Mack Enterpris 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.