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Skylark Device & Systems Co., Ltd.

✅ Low Risk

FEI: 3002808181 • Taipei • TAIWAN

FEI

FEI Number

3002808181

📍

Location

Taipei

🇹🇼

Country

TAIWAN
🏢

Address

34, Sec. 3, 4 F; Chung Shan North Road, Taipei, , Taiwan

Low Risk

FDA Import Risk Assessment

16.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
1
Unique Violations
9/23/2005
Latest Refusal
9/23/2005
Earliest Refusal

Score Breakdown

Violation Severity
30.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

3411×

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

DateProductViolationsDivision
9/23/2005
84GZJSTIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF
341REGISTERED
Chicago District Office (CHI-DO)

Frequently Asked Questions

What is Skylark Device & Systems Co., Ltd.'s FDA import refusal history?

Skylark Device & Systems Co., Ltd. (FEI: 3002808181) has 1 FDA import refusal record(s) in our database, spanning from 9/23/2005 to 9/23/2005.

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. Skylark Device & Systems Co., Ltd.'s FEI number is 3002808181.

What types of violations has Skylark Device & Systems Co., Ltd. received?

Skylark Device & Systems 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 Skylark Device & Systems Co., Ltd. come from?

All FDA import refusal data for Skylark Device & Systems 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.