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Guangzhou Beila Electrical Tech

⚠️ Moderate Risk

FEI: 3010444824 • Guangzhou, Guangdong • CHINA

FEI

FEI Number

3010444824

📍

Location

Guangzhou, Guangdong

🇨🇳

Country

CHINA
🏢

Address

3 Number Fl 2nd, Leshan Road; Fanyu, Guangzhou, Guangdong, China

Moderate Risk

FDA Import Risk Assessment

27.0
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
11/8/2013
Latest Refusal
11/8/2013
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

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
11/8/2013
79OOKDERMAL COOLING PACK/VACUUM/MASSAGER
16DIRECTIONS
3741FRNMFGREG
508NO 510(K)
Seattle District Office (SEA-DO)

Frequently Asked Questions

What is Guangzhou Beila Electrical Tech's FDA import refusal history?

Guangzhou Beila Electrical Tech (FEI: 3010444824) has 1 FDA import refusal record(s) in our database, spanning from 11/8/2013 to 11/8/2013.

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. Guangzhou Beila Electrical Tech's FEI number is 3010444824.

What types of violations has Guangzhou Beila Electrical Tech received?

Guangzhou Beila Electrical Tech has been cited for 3 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 Guangzhou Beila Electrical Tech come from?

All FDA import refusal data for Guangzhou Beila Electrical Tech 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.