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WUHAN CHUANGHENG LASER EQUIPMENT

⚠️ Moderate Risk

FEI: 3025394761 • Wuhan • CHINA

FEI

FEI Number

3025394761

📍

Location

Wuhan

🇨🇳

Country

CHINA
🏢

Address

2101 Chuangxinghui Free, , Wuhan, , China

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
1
Unique Violations
1/26/2023
Latest Refusal
1/26/2023
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
11.2×30%
Recency
26.8×20%
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

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
1/26/2023
95RFELASER CUTTER, MATERIAL PROCESSING LASER PRODUCTS
476NO REGISTR
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is WUHAN CHUANGHENG LASER EQUIPMENT's FDA import refusal history?

WUHAN CHUANGHENG LASER EQUIPMENT (FEI: 3025394761) has 1 FDA import refusal record(s) in our database, spanning from 1/26/2023 to 1/26/2023.

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. WUHAN CHUANGHENG LASER EQUIPMENT's FEI number is 3025394761.

What types of violations has WUHAN CHUANGHENG LASER EQUIPMENT received?

WUHAN CHUANGHENG LASER EQUIPMENT 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 WUHAN CHUANGHENG LASER EQUIPMENT come from?

All FDA import refusal data for WUHAN CHUANGHENG LASER EQUIPMENT 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.