Pt Buana Adhi Gemilang
FDA import alert and refusal historySurabaya, IndonesiaFEI 3012300057
As of October 26, 2026, Pt Buana Adhi Gemilang is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on April 16, 2018, most often for directions (DIRECTIONS).
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) · DIRECTIONS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pt Buana Adhi Gemilang
3 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 3 lines in one entry: Kratom (herbal and botanicals, not teas ii)DIRECTIONSEntry AEK-2166297-5Show 3 linesHide lines
- Refused, Kratom (herbal and botanicals, not teas ii)DIRECTIONSEntry AEK-2166297-5Source
- Refused, Kratom (herbal and botanicals, not teas ii)DIRECTIONSEntry AEK-2166297-5Source
- Refused, Kratom (herbal and botanicals, not teas ii)DIRECTIONSEntry AEK-2166297-5Source
Refusal charges, in plain English
- DIRECTIONS3 refused lines
DIRECTIONS
Questions about Pt Buana Adhi Gemilang
- Is Pt Buana Adhi Gemilang on an FDA import alert?
- No listing for Pt Buana Adhi Gemilang 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 Pt Buana Adhi Gemilang?
- Yes. FDA refused 3 shipment lines from Pt Buana Adhi Gemilang on April 16, 2018. The most recent, on April 16, 2018, was kratom (herbal and botanicals, not teas ii), charged as DIRECTIONS (directions).
- Why did FDA refuse Pt Buana Adhi Gemilang's shipments?
- The most frequent charge is DIRECTIONS (directions, 3 lines).
- What is Pt Buana Adhi Gemilang's FEI number?
- Pt Buana Adhi Gemilang's FDA Establishment Identifier (FEI) is 3012300057.
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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.