ImportRefusal LogoImportRefusal

DONGGUAN MAU GEE I

⚠️ Moderate Risk

FEI: 3016708046 • Dong Guan • CHINA

FEI

FEI Number

3016708046

📍

Location

Dong Guan

🇨🇳

Country

CHINA
🏢

Address

338 Fukang Road D, , Dong Guan, , China

Moderate Risk

FDA Import Risk Assessment

29.1
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
9/21/2020
Latest Refusal
9/21/2020
Earliest Refusal

Score Breakdown

Violation Severity
62.0×40%
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

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

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).

4791×

DV QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.

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
9/21/2020
80QKUNON-NIOSH-APPROVED DISPOSABLE FILTERING FACEPIECE RESPIRATORS (FFRS)
223FALSE
237NO PMA
341REGISTERED
479DV QUALITY
508NO 510(K)
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is DONGGUAN MAU GEE I's FDA import refusal history?

DONGGUAN MAU GEE I (FEI: 3016708046) has 1 FDA import refusal record(s) in our database, spanning from 9/21/2020 to 9/21/2020.

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. DONGGUAN MAU GEE I's FEI number is 3016708046.

What types of violations has DONGGUAN MAU GEE I received?

DONGGUAN MAU GEE I 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 DONGGUAN MAU GEE I come from?

All FDA import refusal data for DONGGUAN MAU GEE I 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.