Emmanuel Ohimhekpen
⚠️ Moderate Risk
FEI: 3005735292 • Lagos, Cross River State • NIGERIA
FEI Number
3005735292
Location
Lagos, Cross River State
Country
NIGERIAAddress
No. 40 Sadiku Street, , Lagos, Cross River State, Nigeria
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/22/2006 | 24TCI31LETTUCE, HEAD (E.G. ICEBERG) (LEAF & STEM VEGETABLE) | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 8/22/2006 | 22BHT02CASABA (CASSABA) MELON, DRIED OR PASTE | 308MFR INSAN | Los Angeles District Office (LOS-DO) |
| 8/22/2006 | 24BHH99BEAN, CORN, PEA, DRIED OR PASTE, N.E.C. (VEGETABLE) | 249FILTHY | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Emmanuel Ohimhekpen's FDA import refusal history?
Emmanuel Ohimhekpen (FEI: 3005735292) has 3 FDA import refusal record(s) in our database, spanning from 8/22/2006 to 8/22/2006.
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. Emmanuel Ohimhekpen's FEI number is 3005735292.
What types of violations has Emmanuel Ohimhekpen received?
Emmanuel Ohimhekpen 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 Emmanuel Ohimhekpen come from?
All FDA import refusal data for Emmanuel Ohimhekpen 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.