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Huanqianbei

⚠️ Moderate Risk

FEI: 3007687507 • Shenzhen • CHINA

FEI

FEI Number

3007687507

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Unit 2708 Block A Oriental Time, , Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

38.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
7/29/2009
Latest Refusal
7/29/2009
Earliest Refusal

Score Breakdown

Violation Severity
85.0×40%
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).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
7/29/2009
89MZXSTIMULATOR, ELECTRICAL FOR SMOKING CESSATION
237NO PMA
75UNAPPROVED
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Huanqianbei's FDA import refusal history?

Huanqianbei (FEI: 3007687507) has 1 FDA import refusal record(s) in our database, spanning from 7/29/2009 to 7/29/2009.

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. Huanqianbei's FEI number is 3007687507.

What types of violations has Huanqianbei received?

Huanqianbei 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 Huanqianbei come from?

All FDA import refusal data for Huanqianbei 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.