Leltek Inc.
⚠️ Moderate Risk
FEI: 3014555455 • New Taipei City • TAIWAN
FEI Number
3014555455
Location
New Taipei City
Country
TAIWANAddress
Xindian District, 6 F.; 3 No. 293, Sec. 1, Beixin Rd., New Taipei City, , Taiwan
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
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/7/2025 | 90ITXTRANSDUCER, ULTRASONIC, DIAGNOSTIC | 341REGISTERED | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is Leltek Inc.'s FDA import refusal history?
Leltek Inc. (FEI: 3014555455) has 1 FDA import refusal record(s) in our database, spanning from 10/7/2025 to 10/7/2025.
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. Leltek Inc.'s FEI number is 3014555455.
What types of violations has Leltek Inc. received?
Leltek Inc. 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 Leltek Inc. come from?
All FDA import refusal data for Leltek Inc. 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.