Cv Leafsync
FDA import alert and refusal historyKalmantan Barat, IndonesiaFEI 3011450464
As of October 26, 2026, Cv Leafsync (Kalmantan Barat, 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 July 15, 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 Cv Leafsync
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 Cv Leafsync
- Is Cv Leafsync on an FDA import alert?
- Yes. As of October 26, 2026, Cv Leafsync 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 July 15, 2015.
- Has FDA refused shipments from Cv Leafsync?
- No FDA import refusals for Cv Leafsync appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Cv Leafsync's FEI number?
- Cv Leafsync's FDA Establishment Identifier (FEI) is 3011450464.
- Can shipments from Cv Leafsync 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 Cv Leafsync 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.