M/S Global Lotus
⚠️ Moderate Risk
FEI: 3008269103 • Gurgaon, Haryana • INDIA
FEI Number
3008269103
Location
Gurgaon, Haryana
Country
INDIAAddress
A - 12/10 Dlf City Phase - I, , Gurgaon, Haryana, India
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
TP VIOL911
This article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product that appears to be in violation of section 911.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/8/2013 | 98B99CIGARETTES, NOT ELSEWHERE CLASSIFIED (N.E.C.) | 3580TP VIOL911 | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is M/S Global Lotus's FDA import refusal history?
M/S Global Lotus (FEI: 3008269103) has 1 FDA import refusal record(s) in our database, spanning from 10/8/2013 to 10/8/2013.
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. M/S Global Lotus's FEI number is 3008269103.
What types of violations has M/S Global Lotus received?
M/S Global Lotus 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 M/S Global Lotus come from?
All FDA import refusal data for M/S Global Lotus 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.