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Victoria Adeyinka

FDA import alert and refusal historyIbadan, NigeriaFEI 3019927061

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

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As of October 26, 2026, Victoria Adeyinka is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 12, 2024, 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
Agave worms, whole edible insects · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Victoria Adeyinka

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

2024

  1. Import refusal
    Refused, Agave worms, whole edible insectsUNAPPROVEDEntry 9RN-1212472-0
    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 Victoria Adeyinka

Is Victoria Adeyinka on an FDA import alert?
No listing for Victoria Adeyinka appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Nigeria page.
Has FDA refused shipments from Victoria Adeyinka?
Yes. FDA refused 1 shipment line from Victoria Adeyinka on June 12, 2024. The most recent, on June 12, 2024, was agave worms, whole edible insects, charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Victoria Adeyinka's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Victoria Adeyinka's FEI number?
Victoria Adeyinka's FDA Establishment Identifier (FEI) is 3019927061.

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Example subjectVictoria Adeyink 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.