PT. Citra Nuansa Buana
FDA import alert and refusal historyBandung, IndonesiaFEI 3010170417
As of October 25, 2026, PT. Citra Nuansa Buana (Bandung, Indonesia) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for kratom; 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 PT. Citra Nuansa Buana
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 54-15red listKratom; Kratom (Herbal and Botanical Teas II, continued); Kratom (Herbal and Botanicals, not Teas II)Source
Questions about PT. Citra Nuansa Buana
- Is PT. Citra Nuansa Buana on an FDA import alert?
- Yes. As of October 25, 2026, PT. Citra Nuansa Buana is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for kratom; 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 PT. Citra Nuansa Buana?
- No FDA import refusals for PT. Citra Nuansa Buana appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is PT. Citra Nuansa Buana's FEI number?
- PT. Citra Nuansa Buana's FDA Establishment Identifier (FEI) is 3010170417.
- Can shipments from PT. Citra Nuansa Buana still enter the U.S.?
- Shipments of kratom; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii) from PT. Citra Nuansa Buana 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.