Transindo Antariksa Logistik
FDA import alert and refusal historyKalimantan Barat, IndonesiaFEI 3026012738
Recorded by FDA as TRANSINDO ANTARIKSA LOGISTIK
As of October 26, 2026, Transindo Antariksa Logistik (Kalimantan Barat, Indonesia) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for mitragyna speciosa (kratom tea), published by FDA on July 27, 2023, 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 Transindo Antariksa Logistik
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 54-15red listMitragyna Speciosa (Kratom tea)Source
Questions about Transindo Antariksa Logistik
- Is Transindo Antariksa Logistik on an FDA import alert?
- Yes. As of October 26, 2026, Transindo Antariksa Logistik is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for mitragyna speciosa (kratom tea); FDA published the listing on July 27, 2023.
- Has FDA refused shipments from Transindo Antariksa Logistik?
- No FDA import refusals for Transindo Antariksa Logistik appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Transindo Antariksa Logistik's FEI number?
- Transindo Antariksa Logistik's FDA Establishment Identifier (FEI) is 3026012738.
- Can shipments from Transindo Antariksa Logistik still enter the U.S.?
- Shipments of mitragyna speciosa (kratom tea) from Transindo Antariksa Logistik 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.