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PENTAX-AOHUA MEDICAL TECHNOLOGIES CO., LTD.

⚠️ Moderate Risk

FEI: 3014718917 • Shanghai, Shanghai • CHINA

FEI

FEI Number

3014718917

📍

Location

Shanghai, Shanghai

🇨🇳

Country

CHINA
🏢

Address

Huaxing Dalou 1 3rd Floor, No. 5 East Ofshenwang Road, Shanghai, Shanghai, China

Moderate Risk

FDA Import Risk Assessment

39.6
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
11/13/2024
Latest Refusal
11/13/2024
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
76.5×20%
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

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
11/13/2024
73BZNCART, EMERGENCY, CARDIOPULMONARY (EXCLUDING EQUIPMENT)
3280FRNMFGREG
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is PENTAX-AOHUA MEDICAL TECHNOLOGIES CO., LTD.'s FDA import refusal history?

PENTAX-AOHUA MEDICAL TECHNOLOGIES CO., LTD. (FEI: 3014718917) has 1 FDA import refusal record(s) in our database, spanning from 11/13/2024 to 11/13/2024.

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. PENTAX-AOHUA MEDICAL TECHNOLOGIES CO., LTD.'s FEI number is 3014718917.

What types of violations has PENTAX-AOHUA MEDICAL TECHNOLOGIES CO., LTD. received?

PENTAX-AOHUA MEDICAL TECHNOLOGIES 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 PENTAX-AOHUA MEDICAL TECHNOLOGIES CO., LTD. come from?

All FDA import refusal data for PENTAX-AOHUA MEDICAL TECHNOLOGIES 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.