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Hangzhou Angiesi Medtech Co Ltd

✅ Low Risk

FEI: 3010191435 • Hangzhou, Zhejiang • CHINA

FEI

FEI Number

3010191435

📍

Location

Hangzhou, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

2nd Floor, 1st 320 Zhenhua Road, Hangzhou, Zhejiang, China

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
2/28/2017
Latest Refusal
2/28/2017
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
2/28/2017
79FZPCLIP, IMPLANTABLE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Hangzhou Angiesi Medtech Co Ltd's FDA import refusal history?

Hangzhou Angiesi Medtech Co Ltd (FEI: 3010191435) has 1 FDA import refusal record(s) in our database, spanning from 2/28/2017 to 2/28/2017.

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. Hangzhou Angiesi Medtech Co Ltd's FEI number is 3010191435.

What types of violations has Hangzhou Angiesi Medtech Co Ltd received?

Hangzhou Angiesi Medtech Co Ltd 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 Hangzhou Angiesi Medtech Co Ltd come from?

All FDA import refusal data for Hangzhou Angiesi Medtech 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.