AJAYI TOLULOPE
⚠️ High Risk
FEI: 3021918851 • Mafoluku • NIGERIA
FEI Number
3021918851
Location
Mafoluku
Country
NIGERIAAddress
54 Mafoluku Road, , Mafoluku, , Nigeria
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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/15/2022 | 60QDY67LIDOCAINE (ANESTHETIC) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 4/15/2022 | 62LDY50METRONIDAZOLE HYDROCHLORIDE (ANTI-PROTOZOAL, A-LEISHMANIAL, ANTI-MALARIAL) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 4/15/2022 | 61GDY55SULFAMETHAZINE (ANTI-BACTERIAL) (NOT ANTIBIOTIC) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 4/15/2022 | 56YDY99ANTIBIOTIC N.E.C. | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
| 4/15/2022 | 63HDY12MAGNESIUM CITRATE(SOL) (CATHARTIC) | 75UNAPPROVED | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is AJAYI TOLULOPE's FDA import refusal history?
AJAYI TOLULOPE (FEI: 3021918851) has 5 FDA import refusal record(s) in our database, spanning from 4/15/2022 to 4/15/2022.
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. AJAYI TOLULOPE's FEI number is 3021918851.
What types of violations has AJAYI TOLULOPE received?
AJAYI TOLULOPE 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 AJAYI TOLULOPE come from?
All FDA import refusal data for AJAYI TOLULOPE 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.