I B SABBA S.A.
⚠️ Moderate Risk
FEI: 3004314751 • Manaus, Amazonas • BRAZIL
FEI Number
3004314751
Location
Manaus, Amazonas
Country
BRAZILAddress
Rua Pajura 865 Dist. Industrial, , Manaus, Amazonas, Brazil
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
AFLATOXIN
The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/7/2010 | 23AAH02BRAZIL NUT, IN SHELL | 297AFLATOXIN | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is I B SABBA S.A.'s FDA import refusal history?
I B SABBA S.A. (FEI: 3004314751) has 1 FDA import refusal record(s) in our database, spanning from 12/7/2010 to 12/7/2010.
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. I B SABBA S.A.'s FEI number is 3004314751.
What types of violations has I B SABBA S.A. received?
I B SABBA S.A. has been cited for 1 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 I B SABBA S.A. come from?
All FDA import refusal data for I B SABBA S.A. 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.