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DONG RI ELECTRICAL EQUIPMENT COLTD

⚠️ Moderate Risk

FEI: 3017210570 • Dongguan, Guangdong • CHINA

FEI

FEI Number

3017210570

📍

Location

Dongguan, Guangdong

🇨🇳

Country

CHINA
🏢

Address

Gaobu Caoduncun, Caodun Industrial Area Gaobuzhen, Dongguan, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

43.3
LowModerateHighCritical

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

Statistics

7
Total Refusals
4
Unique Violations
1/14/2022
Latest Refusal
2/3/2021
Earliest Refusal

Score Breakdown

Violation Severity
62.8×40%
Refusal Volume
33.5×30%
Recency
5.8×20%
Frequency
70.0×10%
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

5087×

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.

1184×

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).

32804×

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.

2373×

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).

Refusal History

DateProductViolationsDivision
1/14/2022
80LRJDISINFECTANT, MEDICAL DEVICES
237NO PMA
508NO 510(K)
Division of West Coast Imports (DWCI)
1/7/2022
80LRJDISINFECTANT, MEDICAL DEVICES
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of West Coast Imports (DWCI)
1/7/2022
80LRJDISINFECTANT, MEDICAL DEVICES
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of West Coast Imports (DWCI)
1/7/2022
80LRJDISINFECTANT, MEDICAL DEVICES
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of West Coast Imports (DWCI)
1/6/2022
80LRJDISINFECTANT, MEDICAL DEVICES
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of West Coast Imports (DWCI)
2/3/2021
80LRJDISINFECTANT, MEDICAL DEVICES
237NO PMA
508NO 510(K)
Division of West Coast Imports (DWCI)
2/3/2021
80LRJDISINFECTANT, MEDICAL DEVICES
237NO PMA
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is DONG RI ELECTRICAL EQUIPMENT COLTD's FDA import refusal history?

DONG RI ELECTRICAL EQUIPMENT COLTD (FEI: 3017210570) has 7 FDA import refusal record(s) in our database, spanning from 2/3/2021 to 1/14/2022.

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. DONG RI ELECTRICAL EQUIPMENT COLTD's FEI number is 3017210570.

What types of violations has DONG RI ELECTRICAL EQUIPMENT COLTD received?

DONG RI ELECTRICAL EQUIPMENT COLTD 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 DONG RI ELECTRICAL EQUIPMENT COLTD come from?

All FDA import refusal data for DONG RI ELECTRICAL EQUIPMENT COLTD 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.