Aboagye Agyemang
FDA import alert and refusal historyGent, BelgiumFEI 3018011811
Recorded by FDA as ABOAGYE AGYEMANG
As of October 26, 2026, Aboagye Agyemang is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 24, 2021, 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
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Aboagye Agyemang
1 record, newest first. Each line links to the FDA page it came from.
2021
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-4415141-5Source
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 Aboagye Agyemang
- Is Aboagye Agyemang on an FDA import alert?
- No listing for Aboagye Agyemang 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 Aboagye Agyemang?
- Yes. FDA refused 1 shipment line from Aboagye Agyemang on March 24, 2021. The most recent, on March 24, 2021, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Aboagye Agyemang's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Aboagye Agyemang's FEI number?
- Aboagye Agyemang's FDA Establishment Identifier (FEI) is 3018011811.
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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.