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IMOTION (SHANGHAI) PRODUCT DESIGN COMPANY LIMITED

⚠️ Moderate Risk

FEI: 3010006343 • Pudongxin, Shanghai • CHINA

FEI

FEI Number

3010006343

📍

Location

Pudongxin, Shanghai

🇨🇳

Country

CHINA
🏢

Address

Building 4, No 315 Jingye Road, Pudongxin, Shanghai, China

Moderate Risk

FDA Import Risk Assessment

35.9
LowModerateHighCritical

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

Statistics

9
Total Refusals
3
Unique Violations
2/16/2021
Latest Refusal
9/1/2020
Earliest Refusal

Score Breakdown

Violation Severity
39.3×40%
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

3418×

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).

32805×

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.

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).

Refusal History

DateProductViolationsDivision
2/16/2021
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
2/4/2021
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
341REGISTERED
Division of West Coast Imports (DWCI)
2/4/2021
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
341REGISTERED
Division of West Coast Imports (DWCI)
1/19/2021
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
1/13/2021
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
1/12/2021
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
3280FRNMFGREG
341REGISTERED
Division of West Coast Imports (DWCI)
11/30/2020
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
Division of West Coast Imports (DWCI)
9/1/2020
89LYGMASSAGER, THERAPEUTIC, MANUAL
341REGISTERED
Division of West Coast Imports (DWCI)
9/1/2020
89LYGMASSAGER, THERAPEUTIC, MANUAL
341REGISTERED
Division of West Coast Imports (DWCI)

Frequently Asked Questions

What is IMOTION (SHANGHAI) PRODUCT DESIGN COMPANY LIMITED's FDA import refusal history?

IMOTION (SHANGHAI) PRODUCT DESIGN COMPANY LIMITED (FEI: 3010006343) has 9 FDA import refusal record(s) in our database, spanning from 9/1/2020 to 2/16/2021.

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. IMOTION (SHANGHAI) PRODUCT DESIGN COMPANY LIMITED's FEI number is 3010006343.

What types of violations has IMOTION (SHANGHAI) PRODUCT DESIGN COMPANY LIMITED received?

IMOTION (SHANGHAI) PRODUCT DESIGN COMPANY LIMITED has been cited for 3 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 IMOTION (SHANGHAI) PRODUCT DESIGN COMPANY LIMITED come from?

All FDA import refusal data for IMOTION (SHANGHAI) PRODUCT DESIGN COMPANY LIMITED 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.