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RAYSON TECHNOLOGY CO LTD

⚠️ Moderate Risk

FEI: 3014758817 • Shenzhen • CHINA

FEI

FEI Number

3014758817

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

No. 1 Tongfu 1st Road T, , Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

28.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
11/8/2018
Latest Refusal
11/8/2018
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
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.

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.

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
11/8/2018
74DRTMONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM)
118NOT LISTED
3280FRNMFGREG
479DV QUALITY
508NO 510(K)
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is RAYSON TECHNOLOGY CO LTD's FDA import refusal history?

RAYSON TECHNOLOGY CO LTD (FEI: 3014758817) has 1 FDA import refusal record(s) in our database, spanning from 11/8/2018 to 11/8/2018.

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. RAYSON TECHNOLOGY CO LTD's FEI number is 3014758817.

What types of violations has RAYSON TECHNOLOGY CO LTD received?

RAYSON TECHNOLOGY CO LTD has been cited for 4 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 RAYSON TECHNOLOGY CO LTD come from?

All FDA import refusal data for RAYSON TECHNOLOGY 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.