Duga Komerc
⚠️ Moderate Risk
FEI: 3012597446 • Krusevac • SERBIA
FEI Number
3012597446
Location
Krusevac
Country
SERBIAAddress
Jasicki Put 17v, , Krusevac, , Serbia
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
VITAMN LBL
The food appears to be subject to section 411 and its advertising is false or misleading in a material respect or its labeling is in violation of section 411(b)(2).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/15/2016 | 29RFT04BOTTLED WATER WITH FRUIT FLAVORS, NONCARBONATED (NONMEDICINAL) | Los Angeles District Office (LOS-DO) | |
| 11/15/2016 | 29RFT04BOTTLED WATER WITH FRUIT FLAVORS, NONCARBONATED (NONMEDICINAL) | Los Angeles District Office (LOS-DO) | |
| 11/15/2016 | 29RFT04BOTTLED WATER WITH FRUIT FLAVORS, NONCARBONATED (NONMEDICINAL) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Duga Komerc's FDA import refusal history?
Duga Komerc (FEI: 3012597446) has 3 FDA import refusal record(s) in our database, spanning from 11/15/2016 to 11/15/2016.
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. Duga Komerc's FEI number is 3012597446.
What types of violations has Duga Komerc received?
Duga Komerc 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 Duga Komerc come from?
All FDA import refusal data for Duga Komerc 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.