OM EXIM Corporation
⚠️ High Risk
FEI: 3012631771 • Unjha, Gujarat • INDIA
FEI Number
3012631771
Location
Unjha, Gujarat
Country
INDIAAddress
S/24 Shilp Arcade, Sardar Chowk, 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
FOREIGN OB
The article appears to consist in whole or in part of a filthy, putrid, or decomposed substance, or is otherwise unfit for food in that it appears to contain foreign objects.
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.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
POISONOUS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a poisonous or deleterious substance which may render the article injurious to health. Contains:
PB-FOOD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a poisonous or deleterious substance, lead, which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/9/2020 | 28BGH13CINNAMON, CASSIA, GROUND, CRACKED (SPICE) | 251POISONOUS | Division of Northeast Imports (DNEI) |
| 12/4/2019 | 28BGH13CINNAMON, CASSIA, GROUND, CRACKED (SPICE) | 3400PB-FOOD | Division of Northern Border Imports (DNBI) |
| 6/4/2019 | 33LGT99SOFT CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | 218LIST INGRE | Division of West Coast Imports (DWCI) |
| 6/4/2019 | 33LGT99SOFT CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | 218LIST INGRE | Division of West Coast Imports (DWCI) |
| 6/4/2019 | 33LGT99SOFT CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | 218LIST INGRE | Division of West Coast Imports (DWCI) |
| 4/16/2019 | 28AGH54PEPPER,BLACK, WHOLE (SPICE) | Division of West Coast Imports (DWCI) | |
| 4/16/2019 | 28AGH54PEPPER,BLACK, WHOLE (SPICE) | Division of West Coast Imports (DWCI) | |
| 4/16/2019 | 28AGH54PEPPER,BLACK, WHOLE (SPICE) | Division of West Coast Imports (DWCI) | |
| 4/16/2019 | 28BGH54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Division of West Coast Imports (DWCI) | |
| 4/16/2019 | 28BGH54PEPPER, BLACK, GROUND, CRACKED (SPICE) | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is OM EXIM Corporation's FDA import refusal history?
OM EXIM Corporation (FEI: 3012631771) has 10 FDA import refusal record(s) in our database, spanning from 4/16/2019 to 4/9/2020.
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 3012631771.
What types of violations has OM EXIM Corporation received?
OM EXIM Corporation has been cited for 6 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.