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ONETECH MEDICAL EQUIPMENT CO LIM

⚠️ Moderate Risk

FEI: 3013120231 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3013120231

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

19 YINGBIN, , Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
6/6/2017
Latest Refusal
6/6/2017
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

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).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
6/6/2017
76EHDUNIT, X-RAY, EXTRAORAL WITH TIMER
476NO REGISTR
508NO 510(K)
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is ONETECH MEDICAL EQUIPMENT CO LIM's FDA import refusal history?

ONETECH MEDICAL EQUIPMENT CO LIM (FEI: 3013120231) has 1 FDA import refusal record(s) in our database, spanning from 6/6/2017 to 6/6/2017.

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. ONETECH MEDICAL EQUIPMENT CO LIM's FEI number is 3013120231.

What types of violations has ONETECH MEDICAL EQUIPMENT CO LIM received?

ONETECH MEDICAL EQUIPMENT CO LIM 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 ONETECH MEDICAL EQUIPMENT CO LIM come from?

All FDA import refusal data for ONETECH MEDICAL EQUIPMENT CO LIM 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.