Abacous Group
⚠️ Moderate Risk
FEI: 2000016323 • Banjul • GAMBIA
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
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.
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.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/9/2007 | 16AGH10CATFISH, FRESHWATER (E.G. CHANNEL, BLUE, WHITE, YAQUI, BULLHEAD, FLATHEAD CATFISH) | Atlanta District Office (ATL-DO) | |
| 5/9/2007 | 16AGD44TROUT (RAINBOW, BROOK, BROWN, CHAR, STEELHEAD, ETC.) | 9SALMONELLA | Atlanta District Office (ATL-DO) |
| 6/30/2006 | 16EGD03OYSTERS | 251POISONOUS | Atlanta District Office (ATL-DO) |
Frequently Asked Questions
What is Abacous Group's FDA import refusal history?
Abacous Group (FEI: 2000016323) has 3 FDA import refusal record(s) in our database, spanning from 6/30/2006 to 5/9/2007.
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. Abacous Group's FEI number is 2000016323.
What types of violations has Abacous Group received?
Abacous Group 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 Abacous Group come from?
All FDA import refusal data for Abacous Group 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.