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ANHUI RYZUR MEDICAL EQUIPMENT MANUFACTURING CO., LTD

⚠️ Moderate Risk

FEI: 3010360428 • Hefei, Anhui • CHINA

FEI

FEI Number

3010360428

📍

Location

Hefei, Anhui

🇨🇳

Country

CHINA
🏢

Address

Ryzur Medical Industrial Park,South Of Guanhai Road And West Of Susong, Road Economic&Technological Development, Hefei, Anhui, 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
1
Unique Violations
7/1/2020
Latest Refusal
7/1/2020
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

4791×

DV QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.

Refusal History

DateProductViolationsDivision
7/1/2020
80LYUACCESSORY, SURGICAL APPAREL
479DV QUALITY
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is ANHUI RYZUR MEDICAL EQUIPMENT MANUFACTURING CO., LTD's FDA import refusal history?

ANHUI RYZUR MEDICAL EQUIPMENT MANUFACTURING CO., LTD (FEI: 3010360428) has 1 FDA import refusal record(s) in our database, spanning from 7/1/2020 to 7/1/2020.

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. ANHUI RYZUR MEDICAL EQUIPMENT MANUFACTURING CO., LTD's FEI number is 3010360428.

What types of violations has ANHUI RYZUR MEDICAL EQUIPMENT MANUFACTURING CO., LTD received?

ANHUI RYZUR MEDICAL EQUIPMENT MANUFACTURING 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 ANHUI RYZUR MEDICAL EQUIPMENT MANUFACTURING CO., LTD come from?

All FDA import refusal data for ANHUI RYZUR MEDICAL EQUIPMENT MANUFACTURING 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.