African Organic
⚠️ Moderate Risk
FEI: 3004084031 • Kampala • UGANDA
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
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.
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.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/2/2003 | 21TGT02BANANA, DRIED OR PASTE | Seattle District Office (SEA-DO) | |
| 12/2/2003 | 21TGT07PINEAPPLE, DRIED OR PASTE | Seattle District Office (SEA-DO) | |
| 9/29/2003 | 21TGH06PAPAYA, DRIED OR PASTE | 9SALMONELLA | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is African Organic's FDA import refusal history?
African Organic (FEI: 3004084031) has 3 FDA import refusal record(s) in our database, spanning from 9/29/2003 to 12/2/2003.
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. African Organic's FEI number is 3004084031.
What types of violations has African Organic received?
African Organic has been cited for 3 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 African Organic come from?
All FDA import refusal data for African Organic 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.