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Deni I

FDA import alert and refusal historyCibinong, West Java, IndonesiaFEI 3010195524

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Example subjectDeni added to Import Alert 16-129 (red list)

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As of October 26, 2026, Deni I (Cibinong, West Java, Indonesia) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for mitragyna speciosa; acacia mangium and green riau; 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 Deni I

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 listMitragyna Speciosa; Acacia Mangium and Green Riau; Kratom (Herbal and Botanical Teas II, continued); Kratom (Herbal and Botanicals, not Teas II)
    Source

Questions about Deni I

Is Deni I on an FDA import alert?
Yes. As of October 26, 2026, Deni I is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for mitragyna speciosa; acacia mangium and green riau; 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 Deni I?
No FDA import refusals for Deni I appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Deni I's FEI number?
Deni I's FDA Establishment Identifier (FEI) is 3010195524.
Can shipments from Deni I still enter the U.S.?
Shipments of mitragyna speciosa; acacia mangium and green riau; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii) from Deni I 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 subjectDeni 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.