ImportRefusal LogoImportRefusal

Tohkai Precision Electrical Mfy

⚠️ Moderate Risk

FEI: 3003497193 • Shenzhen • CHINA

FEI

FEI Number

3003497193

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Jiazitang Village, Gongming Town Boo An, , Shenzhen, , China

Moderate Risk

FDA Import Risk Assessment

33.9
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
7/3/2002
Latest Refusal
7/3/2002
Earliest Refusal

Score Breakdown

Violation Severity
74.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1261×

FAILS STD

The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

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).

5081×

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.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
7/3/2002
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
126FAILS STD
16DIRECTIONS
237NO PMA
508NO 510(K)
84RX DEVICE
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Tohkai Precision Electrical Mfy's FDA import refusal history?

Tohkai Precision Electrical Mfy (FEI: 3003497193) has 1 FDA import refusal record(s) in our database, spanning from 7/3/2002 to 7/3/2002.

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. Tohkai Precision Electrical Mfy's FEI number is 3003497193.

What types of violations has Tohkai Precision Electrical Mfy received?

Tohkai Precision Electrical Mfy has been cited for 5 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 Tohkai Precision Electrical Mfy come from?

All FDA import refusal data for Tohkai Precision Electrical Mfy 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.