JIANGSU HUACHEN MEDICAL INSTRUME
⚠️ Moderate Risk
FEI: 3013035860 • JIANGSU • CHINA
FEI Number
3013035860
Location
JIANGSU
Country
CHINAAddress
LOUZHUANG INDUSTRIAL PA, JIANGYAN, JIANGSU, , 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
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).
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/5/2020 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 3/12/2020 | 80FLKTHERMOMETER, CLINICAL MERCURY | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 1/31/2020 | 80FLKTHERMOMETER, CLINICAL MERCURY | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 12/17/2019 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 6/19/2019 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 3/29/2019 | 80FLKTHERMOMETER, CLINICAL MERCURY | Division of Southeast Imports (DSEI) | |
| 3/29/2019 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 2/28/2019 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 1/29/2019 | 80FLKTHERMOMETER, CLINICAL MERCURY | Division of Southeast Imports (DSEI) | |
| 1/28/2019 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 4/3/2018 | 80FLKTHERMOMETER, CLINICAL MERCURY | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 3/27/2018 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 3/16/2018 | 80FLKTHERMOMETER, CLINICAL MERCURY | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 2/22/2018 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 10/30/2017 | 80FLKTHERMOMETER, CLINICAL MERCURY | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 7/5/2017 | 80FLKTHERMOMETER, CLINICAL MERCURY | Division of Southeast Imports (DSEI) | |
| 6/8/2017 | 80FLKTHERMOMETER, CLINICAL MERCURY | Division of Southeast Imports (DSEI) | |
| 5/8/2017 | 80FLKTHERMOMETER, CLINICAL MERCURY | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 3/24/2017 | 80FLKTHERMOMETER, CLINICAL MERCURY | Division of Southeast Imports (DSEI) | |
| 2/8/2017 | 80FLKTHERMOMETER, CLINICAL MERCURY | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is JIANGSU HUACHEN MEDICAL INSTRUME's FDA import refusal history?
JIANGSU HUACHEN MEDICAL INSTRUME (FEI: 3013035860) has 20 FDA import refusal record(s) in our database, spanning from 2/8/2017 to 9/5/2020.
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. JIANGSU HUACHEN MEDICAL INSTRUME's FEI number is 3013035860.
What types of violations has JIANGSU HUACHEN MEDICAL INSTRUME received?
JIANGSU HUACHEN MEDICAL INSTRUME 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 JIANGSU HUACHEN MEDICAL INSTRUME come from?
All FDA import refusal data for JIANGSU HUACHEN MEDICAL INSTRUME 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.