LG ELECTRONICS INC MONITOR DIVISION.
⚠️ Moderate Risk
FEI: 3013501671 • Gumi, Gyeongsangbuk • SOUTH KOREA
FEI Number
3013501671
Location
Gumi, Gyeongsangbuk
Country
SOUTH KOREAAddress
Gyeongsangbuk, 77 Sanhodae-Ro, Gumi, Gyeongsangbuk, South Korea
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
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/16/2022 | 90PGYDISPLAY, DIAGNOSTIC RADIOLOGY | 3280FRNMFGREG | Division of Southeast Imports (DSEI) |
| 8/16/2022 | 79FWBCAMERA, TELEVISION, SURGICAL, WITHOUT AUDIO | 3280FRNMFGREG | Division of Southeast Imports (DSEI) |
| 8/16/2022 | 90MQBSOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER) | 3280FRNMFGREG | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is LG ELECTRONICS INC MONITOR DIVISION.'s FDA import refusal history?
LG ELECTRONICS INC MONITOR DIVISION. (FEI: 3013501671) has 3 FDA import refusal record(s) in our database, spanning from 8/16/2022 to 8/16/2022.
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. LG ELECTRONICS INC MONITOR DIVISION.'s FEI number is 3013501671.
What types of violations has LG ELECTRONICS INC MONITOR DIVISION. received?
LG ELECTRONICS INC MONITOR DIVISION. 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 LG ELECTRONICS INC MONITOR DIVISION. come from?
All FDA import refusal data for LG ELECTRONICS INC MONITOR DIVISION. 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.