GENEZA D.O.O
🚨 Critical Risk
FEI: 3016523428 • Kanjiza • SERBIA
FEI Number
3016523428
Location
Kanjiza
Country
SERBIAAddress
Put Narodnih Heroja 17, , Kanjiza, , Serbia
Critical Risk
FDA Import Risk Assessment
This firm has an extensive history of FDA import refusals with severe violations.
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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/8/2025 | 24UYY25SPINACH, DRIED OR PASTE | 241PESTICIDE | Division of Southeast Imports (DSEI) |
| 12/3/2025 | 24UYY25SPINACH, DRIED OR PASTE | 241PESTICIDE | Division of Northeast Imports (DNEI) |
| 11/14/2025 | 24UYY25SPINACH, DRIED OR PASTE | 241PESTICIDE | Division of Southeast Imports (DSEI) |
| 10/9/2025 | 24UYY25SPINACH, DRIED OR PASTE | 241PESTICIDE | Division of Southeast Imports (DSEI) |
| 10/9/2025 | 24UYY25SPINACH, DRIED OR PASTE | 241PESTICIDE | Division of Southeast Imports (DSEI) |
| 10/6/2025 | 24UYY25SPINACH, DRIED OR PASTE | 241PESTICIDE | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is GENEZA D.O.O's FDA import refusal history?
GENEZA D.O.O (FEI: 3016523428) has 6 FDA import refusal record(s) in our database, spanning from 10/6/2025 to 12/8/2025.
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. GENEZA D.O.O's FEI number is 3016523428.
What types of violations has GENEZA D.O.O received?
GENEZA D.O.O 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 GENEZA D.O.O come from?
All FDA import refusal data for GENEZA D.O.O 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.