SupplierRadar

Dh Equisport

FDA import alert and refusal historyMaasmechelen, BelgiumFEI 3013540289

Recorded by FDA as DH EQUISPORT

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Example subjectDh Equispor added to Import Alert 16-129 (red list)

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As of October 26, 2026, Dh Equisport is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 20, 2025, 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
Animal by-products and extracts, n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Dh Equisport

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

2025

  1. Import refusal
    Refused, Animal by-products and extracts, n.e.c.UNAPPROVEDEntry AEK-8191301-2
    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 Dh Equisport

Is Dh Equisport on an FDA import alert?
No listing for Dh Equisport appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Belgium page.
Has FDA refused shipments from Dh Equisport?
Yes. FDA refused 1 shipment line from Dh Equisport on March 20, 2025. The most recent, on March 20, 2025, was animal by-products and extracts, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Dh Equisport's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Dh Equisport's FEI number?
Dh Equisport's FDA Establishment Identifier (FEI) is 3013540289.

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Example subjectDh Equispor 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.