Desky Tri Anugrah
FDA import alert and refusal historyPontianak, IndonesiaFEI 3012021586
As of October 26, 2026, Desky Tri Anugrah is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between November 15, 2016 and April 15, 2019, most often for dietary ingredient without safety assurance (UNSFDIETSP).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Kratom (herbal and botanicals, not teas ii) · UNSFDIETSP
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Desky Tri Anugrah
2 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalRefused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPEntry UPS-4682546-9Source
2016
- Import refusalRefused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPEntry UPS-4676962-6Source
Refusal charges, in plain English
- UNSFDIETSP2 refused lines
Dietary ingredient without safety assurance
The product appeared to be a dietary supplement or dietary ingredient for which there is inadequate information to provide reasonable assurance that it does not present a significant or unreasonable risk of illness or injury.
Questions about Desky Tri Anugrah
- Is Desky Tri Anugrah on an FDA import alert?
- No listing for Desky Tri Anugrah appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
- Has FDA refused shipments from Desky Tri Anugrah?
- Yes. FDA refused 2 shipment lines from Desky Tri Anugrah between November 15, 2016 and April 15, 2019. The most recent, on April 15, 2019, was kratom (herbal and botanicals, not teas ii), charged as UNSFDIETSP (dietary ingredient without safety assurance).
- Why did FDA refuse Desky Tri Anugrah's shipments?
- The most frequent charge is UNSFDIETSP (dietary ingredient without safety assurance, 2 lines).
- What is Desky Tri Anugrah's FEI number?
- Desky Tri Anugrah's FDA Establishment Identifier (FEI) is 3012021586.
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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.