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JOYTECH HEALTHCARE CO. LTD.

⚠️ Moderate Risk

FEI: 3013053058 • Hangzhou, Zhejiang • CHINA

FEI

FEI Number

3013053058

📍

Location

Hangzhou, Zhejiang

🇨🇳

Country

CHINA
🏢

Address

D, Yuhang Economic, No. 365 Wuzhoulu; Yuhang, Hangzhou, Zhejiang, China

Moderate Risk

FDA Import Risk Assessment

46.2
LowModerateHighCritical

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

Statistics

12
Total Refusals
7
Unique Violations
1/14/2025
Latest Refusal
6/8/2020
Earliest Refusal

Score Breakdown

Violation Severity
38.0×40%
Refusal Volume
41.3×30%
Recency
80.2×20%
Frequency
26.1×10%
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

11812×

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).

328012×

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.

34110×

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).

39048×

3904

39058×

3905

5088×

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.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
1/14/2025
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39043904
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/14/2025
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39043904
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/14/2025
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39043904
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/14/2025
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39043904
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/14/2025
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39043904
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/14/2025
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39043904
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/14/2025
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39043904
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/14/2025
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
341REGISTERED
39043904
39053905
508NO 510(K)
Division of Northern Border Imports (DNBI)
1/14/2025
76JESFLOSS, DENTAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
1/14/2025
76JESFLOSS, DENTAL
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of Northern Border Imports (DNBI)
4/17/2023
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)
6/8/2020
74DXNSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is JOYTECH HEALTHCARE CO. LTD.'s FDA import refusal history?

JOYTECH HEALTHCARE CO. LTD. (FEI: 3013053058) has 12 FDA import refusal record(s) in our database, spanning from 6/8/2020 to 1/14/2025.

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. JOYTECH HEALTHCARE CO. LTD.'s FEI number is 3013053058.

What types of violations has JOYTECH HEALTHCARE CO. LTD. received?

JOYTECH HEALTHCARE CO. LTD. has been cited for 7 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 JOYTECH HEALTHCARE CO. LTD. come from?

All FDA import refusal data for JOYTECH HEALTHCARE 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.