CV. Prasada Bali Utama
FDA import alert and refusal historyDenpasar, IndonesiaFEI 3010178249
Recorded by FDA as CV. PRASADA BALI UTAMA
As of October 26, 2026, CV. Prasada Bali Utama (Denpasar, 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); dried mitragyna speciosa, published by FDA on June 16, 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 CV. Prasada Bali Utama
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); Dried Mitragyna SpeciosaSource
Questions about CV. Prasada Bali Utama
- Is CV. Prasada Bali Utama on an FDA import alert?
- Yes. As of October 26, 2026, CV. Prasada Bali Utama 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); dried mitragyna speciosa; FDA published the listing on June 16, 2014.
- Has FDA refused shipments from CV. Prasada Bali Utama?
- No FDA import refusals for CV. Prasada Bali Utama appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is CV. Prasada Bali Utama's FEI number?
- CV. Prasada Bali Utama's FDA Establishment Identifier (FEI) is 3010178249.
- Can shipments from CV. Prasada Bali Utama still enter the U.S.?
- Shipments of kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); dried mitragyna speciosa from CV. Prasada Bali Utama 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.