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Jiangsu Medomics Medical Technology Co., Ltd.

⚠️ Moderate Risk

FEI: 3016621374 • Nanjing, Jiangsu • CHINA

FEI

FEI Number

3016621374

📍

Location

Nanjing, Jiangsu

🇨🇳

Country

CHINA
🏢

Address

Building 01, Phase 6, No.71, Xinghui Road Jiangbei New Area, , Nanjing, Jiangsu, China

Moderate Risk

FDA Import Risk Assessment

36.7
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
7/23/2020
Latest Refusal
4/24/2020
Earliest Refusal

Score Breakdown

Violation Severity
62.2×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

5084×

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.

1182×

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).

32802×

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.

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

Refusal History

DateProductViolationsDivision
7/23/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
508NO 510(K)
Division of Southeast Imports (DSEI)
7/22/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
508NO 510(K)
Division of Northern Border Imports (DNBI)
6/17/2020
83QKOREAGENT, CORONAVIRUS SEROLOGICAL
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
4/24/2020
83QKPCORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
118NOT LISTED
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Jiangsu Medomics Medical Technology Co., Ltd.'s FDA import refusal history?

Jiangsu Medomics Medical Technology Co., Ltd. (FEI: 3016621374) has 4 FDA import refusal record(s) in our database, spanning from 4/24/2020 to 7/23/2020.

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. Jiangsu Medomics Medical Technology Co., Ltd.'s FEI number is 3016621374.

What types of violations has Jiangsu Medomics Medical Technology Co., Ltd. received?

Jiangsu Medomics Medical 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 Jiangsu Medomics Medical Technology Co., Ltd. come from?

All FDA import refusal data for Jiangsu Medomics Medical 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.