Husni
FDA import alert and refusal historyBekasi, IndonesiaFEI 3017110094
Recorded by FDA as HUSNI
As of October 26, 2026, Husni is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between June 17, 2021 and June 22, 2021, 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 Husni
2 records, newest first. Each line links to the FDA page it came from.
2021
- Import refusalRefused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPEntry SCS-1305317-0Source
- Import refusalRefused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPEntry SCS-1305494-7Source
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 Husni
- Is Husni on an FDA import alert?
- No listing for Husni 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 Husni?
- Yes. FDA refused 2 shipment lines from Husni between June 17, 2021 and June 22, 2021. The most recent, on June 22, 2021, was kratom (herbal and botanicals, not teas ii), charged as UNSFDIETSP (dietary ingredient without safety assurance).
- Why did FDA refuse Husni's shipments?
- The most frequent charge is UNSFDIETSP (dietary ingredient without safety assurance, 2 lines).
- What is Husni's FEI number?
- Husni's FDA Establishment Identifier (FEI) is 3017110094.
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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.