AHROSILPROM TOV
⚠️ High Risk
FEI: 3039393998 • Horianivske • UKRAINE
FEI Number
3039393998
Location
Horianivske
Country
UKRAINEAddress
3-A Vul. Nahorna, , Horianivske, , Ukraine
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/25/2025 | 26BCT11MUSTARD OIL SEED STOCK | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is AHROSILPROM TOV's FDA import refusal history?
AHROSILPROM TOV (FEI: 3039393998) has 1 FDA import refusal record(s) in our database, spanning from 11/25/2025 to 11/25/2025.
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. AHROSILPROM TOV's FEI number is 3039393998.
What types of violations has AHROSILPROM TOV received?
AHROSILPROM TOV 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 AHROSILPROM TOV come from?
All FDA import refusal data for AHROSILPROM TOV 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.