OM EXIM CORPORATION
⚠️ High Risk
FEI: 3016414218 • Gujurat • 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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
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 |
|---|---|---|---|
| 5/23/2022 | 28AYY54PEPPER,BLACK, WHOLE (SPICE) | 249FILTHY | Division of Northern Border Imports (DNBI) |
| 5/23/2022 | 28AYY54PEPPER,BLACK, WHOLE (SPICE) | 249FILTHY | Division of Northern Border Imports (DNBI) |
| 4/14/2022 | 21TYY14TAMARIND, DRIED OR PASTE | 249FILTHY | Division of Northern Border Imports (DNBI) |
| 4/8/2022 | 28AYY54PEPPER,BLACK, WHOLE (SPICE) | Division of Northern Border Imports (DNBI) | |
| 4/8/2022 | 28AYY54PEPPER,BLACK, WHOLE (SPICE) | Division of Northern Border Imports (DNBI) |
Frequently Asked Questions
What is OM EXIM CORPORATION's FDA import refusal history?
OM EXIM CORPORATION (FEI: 3016414218) has 5 FDA import refusal record(s) in our database, spanning from 4/8/2022 to 5/23/2022.
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 3016414218.
What types of violations has OM EXIM CORPORATION received?
OM EXIM CORPORATION 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 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.