SupplierRadar

Remora Trading

FDA import alert and refusal historyDubai, United Arab EmiratesFEI 3025608583

Recorded by FDA as REMORA TRADING

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Example subjectRemora Tradin added to Import Alert 16-129 (red list)

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As of October 26, 2026, Remora Trading is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 17, 2023, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Herbals & botanicals (not teas), n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Remora Trading

1 record, newest first. Each line links to the FDA page it came from.

2023

  1. Import refusal
    Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry AEK-2768421-4
    Source

Refusal charges, in plain English

  • UNAPPROVED1 refused line

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Remora Trading

Is Remora Trading on an FDA import alert?
No listing for Remora Trading appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the United Arab Emirates page.
Has FDA refused shipments from Remora Trading?
Yes. FDA refused 1 shipment line from Remora Trading on February 17, 2023. The most recent, on February 17, 2023, was herbals & botanicals (not teas), n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Remora Trading's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Remora Trading's FEI number?
Remora Trading's FDA Establishment Identifier (FEI) is 3025608583.

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Example subjectRemora Tradin added to Import Alert 16-129 (red list)

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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.