OM EXIM CORPORATION
⚠️ High Risk
FEI: 3035369475 • Unjha, Gujarat • INDIA
FEI Number
3035369475
Location
Unjha, Gujarat
Country
INDIAAddress
4942 Trishul Industries, R S No; Opp, Near Iabh Sortex, Unjha, Gujarat, India
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
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/31/2025 | 28BGH15CORIANDER, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of West Coast Imports (DWCI) |
| 12/31/2025 | 28BGH15CORIANDER, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of West Coast Imports (DWCI) |
| 12/31/2025 | 28BGH15CORIANDER, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of West Coast Imports (DWCI) |
| 8/6/2025 | 28BGT49TURMERIC, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northern Border Imports (DNBI) |
| 8/6/2025 | 28BGT15CORIANDER, GROUND, CRACKED (SPICE) | 9SALMONELLA | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is OM EXIM CORPORATION's FDA import refusal history?
OM EXIM CORPORATION (FEI: 3035369475) has 5 FDA import refusal record(s) in our database, spanning from 8/6/2025 to 12/31/2025.
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. OM EXIM CORPORATION's FEI number is 3035369475.
What types of violations has OM EXIM CORPORATION received?
OM EXIM CORPORATION 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 OM EXIM CORPORATION come from?
All FDA import refusal data for OM EXIM CORPORATION 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.