Bokomo Foods
⚠️ Moderate Risk
FEI: 3007767810 • N1 City • SOUTH AFRICA
FEI Number
3007767810
Location
N1 City
Country
SOUTH AFRICAAddress
Bokomo Durban Depotp.O. Box 12910, , N1 City, , South Africa
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
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).
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.
Refusal History
Frequently Asked Questions
What is Bokomo Foods's FDA import refusal history?
Bokomo Foods (FEI: 3007767810) has 1 FDA import refusal record(s) in our database, spanning from 10/2/2009 to 10/2/2009.
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. Bokomo Foods's FEI number is 3007767810.
What types of violations has Bokomo Foods received?
Bokomo Foods has been cited for 2 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 Bokomo Foods come from?
All FDA import refusal data for Bokomo Foods 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.