HUNAN BEI'ER AN'QIN MEDICAL TECHNOLOGY CO., LTD
✅ Low Risk
FEI: 3016689342 • Changsha, Hunan • CHINA
FEI Number
3016689342
Location
Changsha, Hunan
Country
CHINAAddress
No. 502 Juxing Chungye Jidi,No.8 Lujing Road,Changsha High-Tech Development Zone, , Changsha, Hunan, China
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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).
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.
Refusal History
Frequently Asked Questions
What is HUNAN BEI'ER AN'QIN MEDICAL TECHNOLOGY CO., LTD's FDA import refusal history?
HUNAN BEI'ER AN'QIN MEDICAL TECHNOLOGY CO., LTD (FEI: 3016689342) has 1 FDA import refusal record(s) in our database, spanning from 8/19/2020 to 8/19/2020.
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. HUNAN BEI'ER AN'QIN MEDICAL TECHNOLOGY CO., LTD's FEI number is 3016689342.
What types of violations has HUNAN BEI'ER AN'QIN MEDICAL TECHNOLOGY CO., LTD received?
HUNAN BEI'ER AN'QIN MEDICAL TECHNOLOGY CO., LTD 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 HUNAN BEI'ER AN'QIN MEDICAL TECHNOLOGY CO., LTD come from?
All FDA import refusal data for HUNAN BEI'ER AN'QIN MEDICAL TECHNOLOGY 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.