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Noend Industries Company Ltd

⚠️ Moderate Risk

FEI: 3003600006 • Tuen Mun, New Territories • HONG KONG

FEI

FEI Number

3003600006

📍

Location

Tuen Mun, New Territories

🇭🇰

Country

HONG KONG
🏢

Address

No 23 Luk Yuen Street, , Tuen Mun, New Territories, Hong Kong

Moderate Risk

FDA Import Risk Assessment

29.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
5/13/2002
Latest Refusal
5/13/2002
Earliest Refusal

Score Breakdown

Violation Severity
64.0×40%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

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).

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.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
5/13/2002
84GZJSTIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF
16DIRECTIONS
237NO PMA
341REGISTERED
508NO 510(K)
84RX DEVICE
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Noend Industries Company Ltd's FDA import refusal history?

Noend Industries Company Ltd (FEI: 3003600006) has 1 FDA import refusal record(s) in our database, spanning from 5/13/2002 to 5/13/2002.

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. Noend Industries Company Ltd's FEI number is 3003600006.

What types of violations has Noend Industries Company Ltd received?

Noend Industries Company Ltd has been cited for 5 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 Noend Industries Company Ltd come from?

All FDA import refusal data for Noend Industries Company 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.