Droind
FDA import alert and refusal historyChungcheongnam-do, South KoreaFEI 3046439512
As of October 26, 2026, Droind is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 13, 2026, most often for no u.s. adverse event contact on supplement label (NCONTACT).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Ginseng (herbal & botanical teas) · NCONTACT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Droind
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- NCONTACT1 refused line
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
Questions about Droind
- Is Droind on an FDA import alert?
- No listing for Droind appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
- Has FDA refused shipments from Droind?
- Yes. FDA refused 1 shipment line from Droind on August 13, 2026. The most recent, on August 13, 2026, was ginseng (herbal & botanical teas), charged as NCONTACT (no u.s. adverse event contact on supplement label).
- Why did FDA refuse Droind's shipments?
- The most frequent charge is NCONTACT (no u.s. adverse event contact on supplement label, 1 line).
- What is Droind's FEI number?
- Droind's FDA Establishment Identifier (FEI) is 3046439512.
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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.