Mumung Mulharyana
FDA import alert and refusal historyPontianak, IndonesiaFEI 3009605360
As of October 26, 2026, Mumung Mulharyana (Pontianak, Indonesia) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for mitragyna speciosa extract; 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
- 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 Mumung Mulharyana
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 54-15red listMitragyna Speciosa Extract; Kratom (Herbal and Botanical Teas II, continued); Kratom (Herbal and Botanicals, not Teas II)Source
Questions about Mumung Mulharyana
- Is Mumung Mulharyana on an FDA import alert?
- Yes. As of October 26, 2026, Mumung Mulharyana is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for mitragyna speciosa extract; 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 Mumung Mulharyana?
- No FDA import refusals for Mumung Mulharyana appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Mumung Mulharyana's FEI number?
- Mumung Mulharyana's FDA Establishment Identifier (FEI) is 3009605360.
- Can shipments from Mumung Mulharyana still enter the U.S.?
- Shipments of mitragyna speciosa extract; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii) from Mumung Mulharyana 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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