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E Concept Technology Co Ltd

⚠️ Moderate Risk

FEI: 3010975046 • Lantau Island - Cheung Sha, New Territories • HONG KONG

FEI

FEI Number

3010975046

📍

Location

Lantau Island - Cheung Sha, New Territories

🇭🇰

Country

HONG KONG
🏢

Address

788 Cheung Sha Floor 33, Laws Comm Plaza; Wan, Lantau Island - Cheung Sha, New Territories, Hong Kong

Moderate Risk

FDA Import Risk Assessment

29.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
4/9/2015
Latest Refusal
4/9/2015
Earliest Refusal

Score Breakdown

Violation Severity
62.5×40%
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

1181×

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).

23801×

NO PMA/PDP

The article appears to be a class III dev.w/o an approved applic. for premarket approval, and/or a notice of completion of product development protocol filed per section 515(b) or exempt per sect.520(g)(1).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

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
4/9/2015
80LDQDEVICE, GENERAL MEDICAL
118NOT LISTED
2380NO PMA/PDP
3280FRNMFGREG
84RX DEVICE
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is E Concept Technology Co Ltd's FDA import refusal history?

E Concept Technology Co Ltd (FEI: 3010975046) has 1 FDA import refusal record(s) in our database, spanning from 4/9/2015 to 4/9/2015.

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. E Concept Technology Co Ltd's FEI number is 3010975046.

What types of violations has E Concept Technology Co Ltd received?

E Concept Technology Co Ltd has been cited for 4 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 E Concept Technology Co Ltd come from?

All FDA import refusal data for E Concept Technology 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.