FAZLANI EXPORTS PVT LTD
⚠️ High Risk
FEI: 3018041824 • Navi Mumbai, Maharashtra • INDIA
FEI Number
3018041824
Location
Navi Mumbai, Maharashtra
Country
INDIAAddress
Ttc Industrial Area, Gen - 56, Navi Mumbai, Maharashtra, 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
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
Frequently Asked Questions
What is FAZLANI EXPORTS PVT LTD's FDA import refusal history?
FAZLANI EXPORTS PVT LTD (FEI: 3018041824) has 2 FDA import refusal record(s) in our database, spanning from 7/9/2025 to 7/17/2025.
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. FAZLANI EXPORTS PVT LTD's FEI number is 3018041824.
What types of violations has FAZLANI EXPORTS PVT LTD received?
FAZLANI EXPORTS PVT LTD 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 FAZLANI EXPORTS PVT LTD come from?
All FDA import refusal data for FAZLANI EXPORTS PVT LTD 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.