Ayefor Enterprise
⚠️ Moderate Risk
FEI: 3003714144 • Accra • GHANA
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
LACKS N/C
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
USUAL NAME
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/13/2002 | 22AGT99VINE FRUIT, N.E.C. | 328USUAL NAME | Philadelphia District Office (PHI-DO) |
| 9/13/2002 | 02HGT01TAPIOCA STARCH PRODUCT | 321LACKS N/C | Philadelphia District Office (PHI-DO) |
| 9/13/2002 | 02HGT01TAPIOCA STARCH PRODUCT | 321LACKS N/C | Philadelphia District Office (PHI-DO) |
| 9/13/2002 | 28BGT54PEPPER, BLACK, GROUND, CRACKED (SPICE) | 249FILTHY | Philadelphia District Office (PHI-DO) |
| 9/13/2002 | 26CGT05PALM KERNEL OIL, REFINED, SINGLE INGREDIENT | 218LIST INGRE | Philadelphia District Office (PHI-DO) |
Frequently Asked Questions
What is Ayefor Enterprise's FDA import refusal history?
Ayefor Enterprise (FEI: 3003714144) has 5 FDA import refusal record(s) in our database, spanning from 9/13/2002 to 9/13/2002.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Ayefor Enterprise's FEI number is 3003714144.
What types of violations has Ayefor Enterprise received?
Ayefor Enterprise has been cited for 4 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Ayefor Enterprise come from?
All FDA import refusal data for Ayefor Enterprise is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.