MUHAMMED IKBAL GUEMUES
⚠️ Moderate Risk
FEI: 3031531019 • Istanbul • TURKEY
FEI Number
3031531019
Location
Istanbul
Country
TURKEYAddress
Necipfazil Mh Villalarsokak, No22/2 Eren Apt, Istanbul, , Turkey
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
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/23/2024 | 53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
| 9/23/2024 | 53IG01DENTIFRICES (AEROSOL, LIQUID, TOOTHPASTES, TOOTHPOWDERS), WITHOUT FLUORIDE (ORAL HYGIENE PRODUCTS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
| 9/23/2024 | 53JD01BATH SOAPS AND DETERGENTS (NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is MUHAMMED IKBAL GUEMUES's FDA import refusal history?
MUHAMMED IKBAL GUEMUES (FEI: 3031531019) has 3 FDA import refusal record(s) in our database, spanning from 9/23/2024 to 9/23/2024.
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. MUHAMMED IKBAL GUEMUES's FEI number is 3031531019.
What types of violations has MUHAMMED IKBAL GUEMUES received?
MUHAMMED IKBAL GUEMUES 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 MUHAMMED IKBAL GUEMUES come from?
All FDA import refusal data for MUHAMMED IKBAL GUEMUES 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.