M. Ridho Rizki Maulufi Alk
FDA import alert and refusal historyPontianak, IndonesiaFEI 3011504962
As of October 26, 2026, M. Ridho Rizki Maulufi Alk (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 14, 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 M. Ridho Rizki Maulufi Alk
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 M. Ridho Rizki Maulufi Alk
- Is M. Ridho Rizki Maulufi Alk on an FDA import alert?
- Yes. As of October 26, 2026, M. Ridho Rizki Maulufi Alk 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 14, 2015.
- Has FDA refused shipments from M. Ridho Rizki Maulufi Alk?
- No FDA import refusals for M. Ridho Rizki Maulufi Alk appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is M. Ridho Rizki Maulufi Alk's FEI number?
- M. Ridho Rizki Maulufi Alk's FDA Establishment Identifier (FEI) is 3011504962.
- Can shipments from M. Ridho Rizki Maulufi Alk 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 M. Ridho Rizki Maulufi Alk 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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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.