Accu-Tech Co. Ltd
⚠️ Moderate Risk
FEI: 3008792818 • Beijing • CHINA
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
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).
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.
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).
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/26/2012 | 79GEXPOWERED LASER SURGICAL INSTRUMENTS | Seattle District Office (SEA-DO) | |
| 10/6/2011 | 95RZSPOSITIONING MEDICAL LASER PRODUCT | 341REGISTERED | Florida District Office (FLA-DO) |
| 4/17/2011 | 78FECOBTURATOR, FOR ENDOSCOPE | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Accu-Tech Co. Ltd's FDA import refusal history?
Accu-Tech Co. Ltd (FEI: 3008792818) has 3 FDA import refusal record(s) in our database, spanning from 4/17/2011 to 3/26/2012.
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. Accu-Tech Co. Ltd's FEI number is 3008792818.
What types of violations has Accu-Tech Co. Ltd received?
Accu-Tech 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 Accu-Tech Co. Ltd come from?
All FDA import refusal data for Accu-Tech 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.