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Suzhou Kangjie Medical Instrumen

✅ Low Risk

FEI: 3007670356 • Suzhou • CHINA

FEI

FEI Number

3007670356

📍

Location

Suzhou

🇨🇳

Country

CHINA
🏢

Address

129 Weixin Rd, , Suzhou, , China

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
4/5/2013
Latest Refusal
4/5/2013
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

3412×

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
4/5/2013
86HLJOPHTHALMOSCOPE, BATTERY-POWERED
118NOT LISTED
341REGISTERED
Division of Northeast Imports (DNEI)
4/5/2013
86HJOBIOMICROSCOPE, SLIT-LAMP, AC-POWERED
118NOT LISTED
341REGISTERED
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is Suzhou Kangjie Medical Instrumen's FDA import refusal history?

Suzhou Kangjie Medical Instrumen (FEI: 3007670356) has 2 FDA import refusal record(s) in our database, spanning from 4/5/2013 to 4/5/2013.

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. Suzhou Kangjie Medical Instrumen's FEI number is 3007670356.

What types of violations has Suzhou Kangjie Medical Instrumen received?

Suzhou Kangjie Medical Instrumen has been cited for 2 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 Suzhou Kangjie Medical Instrumen come from?

All FDA import refusal data for Suzhou Kangjie Medical Instrumen 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.