LPL (HUI ZHOU) GLOVE CO., LTD.
⚠️ Moderate Risk
FEI: 3008534289 • Huizhou, Guangdong • CHINA
FEI Number
3008534289
Location
Huizhou, Guangdong
Country
CHINAAddress
Factory 6, Daxiaotang Village, Luoyang; Boluoxian, Huizhou, Guangdong, 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 |
|---|---|---|---|
| 12/7/2016 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 477HOLES | Division of Northeast Imports (DNEI) |
| 12/7/2016 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 477HOLES | Division of Northeast Imports (DNEI) |
| 7/11/2016 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 477HOLES | Minneapolis District Office (MIN-DO) |
| 7/11/2016 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 477HOLES | Minneapolis District Office (MIN-DO) |
| 7/11/2016 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 477HOLES | Minneapolis District Office (MIN-DO) |
| 7/11/2016 | 80LYZGLOVE, PATIENT EXAMINATION, VINYL | 477HOLES | Minneapolis District Office (MIN-DO) |
Frequently Asked Questions
What is LPL (HUI ZHOU) GLOVE CO., LTD.'s FDA import refusal history?
LPL (HUI ZHOU) GLOVE CO., LTD. (FEI: 3008534289) has 6 FDA import refusal record(s) in our database, spanning from 7/11/2016 to 12/7/2016.
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. LPL (HUI ZHOU) GLOVE CO., LTD.'s FEI number is 3008534289.
What types of violations has LPL (HUI ZHOU) GLOVE CO., LTD. received?
LPL (HUI ZHOU) GLOVE 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 LPL (HUI ZHOU) GLOVE CO., LTD. come from?
All FDA import refusal data for LPL (HUI ZHOU) GLOVE 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.