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Velobiotics

FDA import alert and refusal historyGermiston, South AfricaFEI 3016762470

Recorded by FDA as VELOBIOTICS

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

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As of October 25, 2026, Velobiotics is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on May 2, 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
Dietary conventional foods, n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Velobiotics

4 records, newest first. Each line links to the FDA page it came from.

2025

  1. Import refusal
    Refused, 4 lines in one entry: Dietary conventional foods, n.e.c.UNAPPROVEDEntry AEK-8365246-9Show 4 lines
    Source

Refusal charges, in plain English

  • UNAPPROVED4 refused lines

    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 Velobiotics

Is Velobiotics on an FDA import alert?
No listing for Velobiotics appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the South Africa page.
Has FDA refused shipments from Velobiotics?
Yes. FDA refused 4 shipment lines from Velobiotics on May 2, 2025. The most recent, on May 2, 2025, was dietary conventional foods, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Velobiotics's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 4 lines).
What is Velobiotics's FEI number?
Velobiotics's FDA Establishment Identifier (FEI) is 3016762470.

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Example subjectVelobiotic 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.