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Shenzhen Mingjin Imp & Exp Co Ltd

⚠️ Moderate Risk

FEI: 3009195910 • Shenzhen • CHINA

FEI

FEI Number

3009195910

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

802a Tianjun Bldg Dongmen S. Road, Luohu, , Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

25.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
9/17/2012
Latest Refusal
9/17/2012
Earliest Refusal

Score Breakdown

Violation Severity
52.0×40%
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

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).

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.

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).

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
9/17/2012
79OHVFOCUSED ULTRASOUND FOR TISSUE HEAT OR MECHANICAL CELLULAR DISRUPTION
118NOT LISTED
3280FRNMFGREG
341REGISTERED
476NO REGISTR
508NO 510(K)
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Shenzhen Mingjin Imp & Exp Co Ltd's FDA import refusal history?

Shenzhen Mingjin Imp & Exp Co Ltd (FEI: 3009195910) has 1 FDA import refusal record(s) in our database, spanning from 9/17/2012 to 9/17/2012.

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. Shenzhen Mingjin Imp & Exp Co Ltd's FEI number is 3009195910.

What types of violations has Shenzhen Mingjin Imp & Exp Co Ltd received?

Shenzhen Mingjin Imp & Exp Co 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 Shenzhen Mingjin Imp & Exp Co Ltd come from?

All FDA import refusal data for Shenzhen Mingjin Imp & Exp 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.