Nihon Chushashin Kogyo Co. Ltd.
⚠️ Moderate Risk
FEI: 5672 • Kita, Tokyo • JAPAN
FEI Number
5672
Location
Kita, Tokyo
Country
JAPANAddress
#28-9 1-Chome, Ojihon-Cho, Kita, Tokyo, Japan
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/26/2025 | 84IKTELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH | Division of Southeast Imports (DSEI) | |
| 3/26/2025 | 84IKTELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH | Division of Southeast Imports (DSEI) | |
| 3/26/2025 | 84IKTELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH | Division of Southeast Imports (DSEI) | |
| 3/26/2025 | 84IKTELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH | Division of Southeast Imports (DSEI) | |
| 3/26/2025 | 84IKTELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH | Division of Southeast Imports (DSEI) | |
| 3/26/2025 | 84IKTELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH | Division of Southeast Imports (DSEI) | |
| 3/26/2025 | 84IKTELECTRODE, NEEDLE, DIAGNOSTIC ELECTROMYOGRAPH | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Nihon Chushashin Kogyo Co. Ltd.'s FDA import refusal history?
Nihon Chushashin Kogyo Co. Ltd. (FEI: 5672) has 7 FDA import refusal record(s) in our database, spanning from 3/26/2025 to 3/26/2025.
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. Nihon Chushashin Kogyo Co. Ltd.'s FEI number is 5672.
What types of violations has Nihon Chushashin Kogyo Co. Ltd. received?
Nihon Chushashin Kogyo Co. Ltd. has been cited for 2 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 Nihon Chushashin Kogyo Co. Ltd. come from?
All FDA import refusal data for Nihon Chushashin Kogyo 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.