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HUIJIANG DISTRICT

⚠️ Moderate Risk

FEI: 3012925638 • GUANDGDONG • CHINA

FEI

FEI Number

3012925638

📍

Location

GUANDGDONG

🇨🇳

Country

CHINA
🏢

Address

HUZHOU CITY, , GUANDGDONG, , China

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
1/31/2017
Latest Refusal
1/31/2017
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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

1971×

COSM COLOR

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).

1981×

COLOR LBLG

The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.

Refusal History

DateProductViolationsDivision
1/31/2017
53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C.
197COSM COLOR
198COLOR LBLG
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is HUIJIANG DISTRICT's FDA import refusal history?

HUIJIANG DISTRICT (FEI: 3012925638) has 1 FDA import refusal record(s) in our database, spanning from 1/31/2017 to 1/31/2017.

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. HUIJIANG DISTRICT's FEI number is 3012925638.

What types of violations has HUIJIANG DISTRICT received?

HUIJIANG DISTRICT 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 HUIJIANG DISTRICT come from?

All FDA import refusal data for HUIJIANG DISTRICT 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.