Mulyadi Pasaribu
FDA import alert and refusal historyMedan, IndonesiaFEI 3009527992
As of October 26, 2026, Mulyadi Pasaribu (Medan, Indonesia) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); mitragyna speciosa, 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 Mulyadi Pasaribu
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 54-15red listKratom (Herbal and Botanical Teas II, continued); Kratom (Herbal and Botanicals, not Teas II); Mitragyna SpeciosaSource
Questions about Mulyadi Pasaribu
- Is Mulyadi Pasaribu on an FDA import alert?
- Yes. As of October 26, 2026, Mulyadi Pasaribu is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); mitragyna speciosa; FDA published the listing on February 28, 2014.
- Has FDA refused shipments from Mulyadi Pasaribu?
- No FDA import refusals for Mulyadi Pasaribu appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Mulyadi Pasaribu's FEI number?
- Mulyadi Pasaribu's FDA Establishment Identifier (FEI) is 3009527992.
- Can shipments from Mulyadi Pasaribu still enter the U.S.?
- Shipments of kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); mitragyna speciosa from Mulyadi Pasaribu 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.