Rudi Hartona
FDA import alert and refusal historyPontianak, IndonesiaFEI 3011337990
As of October 26, 2026, Rudi Hartona (Pontianak, Indonesia) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for mitragyna speciosa (kratom); kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii), published by FDA on October 7, 2015, 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 54-15 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Rudi Hartona
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 54-15red listMitragyna Speciosa (Kratom); Kratom (Herbal and Botanical Teas II, continued); Kratom (Herbal and Botanicals, not Teas II)Source
Questions about Rudi Hartona
- Is Rudi Hartona on an FDA import alert?
- Yes. As of October 26, 2026, Rudi Hartona is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for mitragyna speciosa (kratom); kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); FDA published the listing on October 7, 2015.
- Has FDA refused shipments from Rudi Hartona?
- No FDA import refusals for Rudi Hartona appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Rudi Hartona's FEI number?
- Rudi Hartona's FDA Establishment Identifier (FEI) is 3011337990.
- Can shipments from Rudi Hartona still enter the U.S.?
- Shipments of mitragyna speciosa (kratom); kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii) from Rudi Hartona 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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