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GUANGZHOU XINXIANG

✅ Low Risk

FEI: 3013158912 • Guangzhou • CHINA

FEI

FEI Number

3013158912

📍

Location

Guangzhou

🇨🇳

Country

CHINA
🏢

Address

NO 42 Lanhua Stree, , Guangzhou, , China

Low Risk

FDA Import Risk Assessment

22.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
2
Unique Violations
3/10/2017
Latest Refusal
3/10/2017
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
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

2781×

NO TAG

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
3/10/2017
95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL
278NO TAG
476NO REGISTR
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is GUANGZHOU XINXIANG's FDA import refusal history?

GUANGZHOU XINXIANG (FEI: 3013158912) has 1 FDA import refusal record(s) in our database, spanning from 3/10/2017 to 3/10/2017.

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 XINXIANG's FEI number is 3013158912.

What types of violations has GUANGZHOU XINXIANG received?

GUANGZHOU XINXIANG 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 GUANGZHOU XINXIANG come from?

All FDA import refusal data for GUANGZHOU XINXIANG 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.