Mathur Exports
✅ Low Risk
FEI: 3004644811 • New Delhi • INDIA
FEI Number
3004644811
Location
New Delhi
Country
INDIAAddress
1st Floor, 1115 Main Bazar Pahargenj, , New Delhi, , India
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity 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
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/16/2006 | 53EC01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING) | 475COSMETLBLG | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Mathur Exports's FDA import refusal history?
Mathur Exports (FEI: 3004644811) has 1 FDA import refusal record(s) in our database, spanning from 10/16/2006 to 10/16/2006.
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. Mathur Exports's FEI number is 3004644811.
What types of violations has Mathur Exports received?
Mathur Exports 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 Mathur Exports come from?
All FDA import refusal data for Mathur Exports 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.