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Jingbo Jiangdong Gongfeng Company

⚠️ Moderate Risk

FEI: 3004918319 • Ningbo, Zhejiang • CHINA

FEI

FEI Number

3004918319

📍

Location

Ningbo, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

16 South Baizhang Street, , Ningbo, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

34.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
9/26/2005
Latest Refusal
9/26/2005
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
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

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).

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
9/26/2005
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
237NO PMA
508NO 510(K)
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Jingbo Jiangdong Gongfeng Company's FDA import refusal history?

Jingbo Jiangdong Gongfeng Company (FEI: 3004918319) has 1 FDA import refusal record(s) in our database, spanning from 9/26/2005 to 9/26/2005.

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. Jingbo Jiangdong Gongfeng Company's FEI number is 3004918319.

What types of violations has Jingbo Jiangdong Gongfeng Company received?

Jingbo Jiangdong Gongfeng Company has been cited for 2 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 Jingbo Jiangdong Gongfeng Company come from?

All FDA import refusal data for Jingbo Jiangdong Gongfeng Company 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.