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JICHUN MEDICAL DEVICES CO LTD

⚠️ Moderate Risk

FEI: 3013568429 • JIANGSU • CHINA

FEI

FEI Number

3013568429

📍

Location

JIANGSU

🇨🇳

Country

CHINA
🏢

Address

ZHENGLU TOWN, , CHANGZHOU, JIANGSU, , China

Moderate Risk

FDA Import Risk Assessment

40.1
LowModerateHighCritical

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

Statistics

9
Total Refusals
4
Unique Violations
3/1/2018
Latest Refusal
3/1/2018
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

1189×

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).

32809×

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.

3419×

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).

5089×

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
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
3/1/2018
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is JICHUN MEDICAL DEVICES CO LTD's FDA import refusal history?

JICHUN MEDICAL DEVICES CO LTD (FEI: 3013568429) has 9 FDA import refusal record(s) in our database, spanning from 3/1/2018 to 3/1/2018.

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. JICHUN MEDICAL DEVICES CO LTD's FEI number is 3013568429.

What types of violations has JICHUN MEDICAL DEVICES CO LTD received?

JICHUN MEDICAL DEVICES 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 JICHUN MEDICAL DEVICES CO LTD come from?

All FDA import refusal data for JICHUN MEDICAL DEVICES 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.