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Meda Co., Ltd.

⚠️ Moderate Risk

FEI: 3006540052 • Tianjin, Tianjin • CHINA

FEI

FEI Number

3006540052

📍

Location

Tianjin, Tianjin

🇨🇳

Country

CHINA
🏢

Address

F2c, F3d, F4c, F5, F6c, Building C2, Xinmao Science Skill Park, Huayuan Industry Development Area, Tianjin, Tianjin, China

Moderate Risk

FDA Import Risk Assessment

25.1
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
11/8/2021
Latest Refusal
8/1/2012
Earliest Refusal

Score Breakdown

Violation Severity
41.4×40%
Refusal Volume
25.9×30%
Recency
1.7×20%
Frequency
4.3×10%
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

3414×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

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.

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
11/8/2021
79NTBSYSTEM, ABLATION, ULTRASOUND AND ACCESSORIES
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
8/1/2012
86HLMINSTRUMENT, MEASURING, LENS, AC-POWERED
341REGISTERED
Florida District Office (FLA-DO)
8/1/2012
86HLMINSTRUMENT, MEASURING, LENS, AC-POWERED
341REGISTERED
Florida District Office (FLA-DO)
8/1/2012
86HLMINSTRUMENT, MEASURING, LENS, AC-POWERED
341REGISTERED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Meda Co., Ltd.'s FDA import refusal history?

Meda Co., Ltd. (FEI: 3006540052) has 4 FDA import refusal record(s) in our database, spanning from 8/1/2012 to 11/8/2021.

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. Meda Co., Ltd.'s FEI number is 3006540052.

What types of violations has Meda Co., Ltd. received?

Meda 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 Meda Co., Ltd. come from?

All FDA import refusal data for Meda 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.