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Wenzhou Kindcare Plastic & Metals Product Co., Ltd.

⚠️ Moderate Risk

FEI: 3004784770 • Wenzhoushi, Zhejiangsheng • CHINA

FEI

FEI Number

3004784770

📍

Location

Wenzhoushi, Zhejiangsheng

🇨🇳

Country

CHINA
🏢

Address

Zone 33 Dongyangxilu, , Wenzhoushi, Zhejiangsheng, China

Moderate Risk

FDA Import Risk Assessment

26.1
LowModerateHighCritical

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

Statistics

4
Total Refusals
4
Unique Violations
8/11/2020
Latest Refusal
7/17/2015
Earliest Refusal

Score Breakdown

Violation Severity
43.8×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
7.9×10%
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

1183×

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.

3332×

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.

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

Refusal History

DateProductViolationsDivision
8/11/2020
74LDESTETHOSCOPE, MANUAL
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
7/28/2020
74DXQCUFF, BLOOD-PRESSURE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
7/25/2017
74LDESTETHOSCOPE, MANUAL
118NOT LISTED
223FALSE
333LACKS FIRM
Division of Southeast Imports (DSEI)
7/17/2015
74LDESTETHOSCOPE, MANUAL
333LACKS FIRM
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Wenzhou Kindcare Plastic & Metals Product Co., Ltd.'s FDA import refusal history?

Wenzhou Kindcare Plastic & Metals Product Co., Ltd. (FEI: 3004784770) has 4 FDA import refusal record(s) in our database, spanning from 7/17/2015 to 8/11/2020.

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. Wenzhou Kindcare Plastic & Metals Product Co., Ltd.'s FEI number is 3004784770.

What types of violations has Wenzhou Kindcare Plastic & Metals Product Co., Ltd. received?

Wenzhou Kindcare Plastic & Metals Product 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 Wenzhou Kindcare Plastic & Metals Product Co., Ltd. come from?

All FDA import refusal data for Wenzhou Kindcare Plastic & Metals Product 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.