Rebecca Amoah Enterprise
⚠️ Moderate Risk
FEI: 3005180833 • 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
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/21/2005 | 29BYY99CARBONATED SOFT DRINK, N.E.C. | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 9/21/2005 | 02HFH02CORN STARCH | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 9/21/2005 | 02HFH02CORN STARCH | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 9/21/2005 | 02HFH02CORN STARCH | 482NUTRIT LBL | New York District Office (NYK-DO) |
| 9/21/2005 | 54ACL90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 473LABELING | New York District Office (NYK-DO) |
| 9/21/2005 | 54ACL90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 473LABELING | New York District Office (NYK-DO) |
| 9/21/2005 | 54ACL90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN) | 473LABELING | New York District Office (NYK-DO) |
| 9/21/2005 | 02HFH02CORN STARCH | 62NEEDS FCE | New York District Office (NYK-DO) |
| 9/21/2005 | 29BYY99CARBONATED SOFT DRINK, N.E.C. | 11UNSAFE COL | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Rebecca Amoah Enterprise's FDA import refusal history?
Rebecca Amoah Enterprise (FEI: 3005180833) has 9 FDA import refusal record(s) in our database, spanning from 9/21/2005 to 9/21/2005.
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. Rebecca Amoah Enterprise's FEI number is 3005180833.
What types of violations has Rebecca Amoah Enterprise received?
Rebecca Amoah 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 Rebecca Amoah Enterprise come from?
All FDA import refusal data for Rebecca Amoah 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.