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Zhejiang Zhongda Group Co., Ltd.

⚠️ Moderate Risk

FEI: 3004010853 • Hangzhou • CHINA

FEI

FEI Number

3004010853

📍

Location

Hangzhou

🇨🇳

Country

CHINA
🏢

Address

Hao Ge Bldg. Shang Tang Rm 504, 39 Road, Hangzhou, , China

Moderate Risk

FDA Import Risk Assessment

44.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
8/12/2003
Latest Refusal
8/12/2003
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
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

2411×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

Refusal History

DateProductViolationsDivision
8/12/2003
24AGT51PEAS
241PESTICIDE
New York District Office (NYK-DO)

Frequently Asked Questions

What is Zhejiang Zhongda Group Co., Ltd.'s FDA import refusal history?

Zhejiang Zhongda Group Co., Ltd. (FEI: 3004010853) has 1 FDA import refusal record(s) in our database, spanning from 8/12/2003 to 8/12/2003.

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. Zhejiang Zhongda Group Co., Ltd.'s FEI number is 3004010853.

What types of violations has Zhejiang Zhongda Group Co., Ltd. received?

Zhejiang Zhongda Group Co., Ltd. has been cited for 1 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 Zhejiang Zhongda Group Co., Ltd. come from?

All FDA import refusal data for Zhejiang Zhongda Group Co., Ltd. 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.