Shanghai Lanfan Co Ltd
⚠️ Moderate Risk
FEI: 3006737380 • Shanghai, Shanghai • CHINA
FEI Number
3006737380
Location
Shanghai, Shanghai
Country
CHINAAddress
Huaxia Bank Tower 2002, 256 Pudongnanlu, Shanghai, Shanghai, China
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
HOLES
The quality of the article falls below that which it purports or is represented to possess, in that the devices contain defects/holes.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/19/2008 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 477HOLES | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Shanghai Lanfan Co Ltd's FDA import refusal history?
Shanghai Lanfan Co Ltd (FEI: 3006737380) has 1 FDA import refusal record(s) in our database, spanning from 12/19/2008 to 12/19/2008.
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. Shanghai Lanfan Co Ltd's FEI number is 3006737380.
What types of violations has Shanghai Lanfan Co Ltd received?
Shanghai Lanfan Co 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 Shanghai Lanfan Co Ltd come from?
All FDA import refusal data for Shanghai Lanfan Co 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.