Astri Megi
FDA import alert and refusal historyJakarta Selatan, IndonesiaFEI 3020063028
Recorded by FDA as ASTRI MEGI
As of October 25, 2026, Astri Megi is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on October 5, 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 Astri Megi
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-7473964-2Source
- Import refusalRefused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPEntry SCS-7468825-2Source
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 Astri Megi
- Is Astri Megi on an FDA import alert?
- No listing for Astri Megi appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Indonesia page.
- Has FDA refused shipments from Astri Megi?
- Yes. FDA refused 2 shipment lines from Astri Megi on October 5, 2021. The most recent, on October 5, 2021, was kratom (herbal and botanicals, not teas ii), charged as UNSFDIETSP (dietary ingredient without safety assurance).
- Why did FDA refuse Astri Megi's shipments?
- The most frequent charge is UNSFDIETSP (dietary ingredient without safety assurance, 2 lines).
- What is Astri Megi's FEI number?
- Astri Megi's FDA Establishment Identifier (FEI) is 3020063028.
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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.