SHENZHEN MEILI MEDICAL DEVICES CO.,LTD
⚠️ Moderate Risk
FEI: 3016712997 • Shenzhen City, Guangdong • CHINA
FEI Number
3016712997
Location
Shenzhen City, Guangdong
Country
CHINAAddress
Of Baishixia Community,Fuyong Street,Bao'An District Room 301, No. 33 Rifu Road; East District, Shenzhen City, Guangdong, 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
DV QUALITY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.
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 SHENZHEN MEILI MEDICAL DEVICES CO.,LTD's FDA import refusal history?
SHENZHEN MEILI MEDICAL DEVICES CO.,LTD (FEI: 3016712997) has 1 FDA import refusal record(s) in our database, spanning from 7/21/2020 to 7/21/2020.
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. SHENZHEN MEILI MEDICAL DEVICES CO.,LTD's FEI number is 3016712997.
What types of violations has SHENZHEN MEILI MEDICAL DEVICES CO.,LTD received?
SHENZHEN MEILI MEDICAL DEVICES 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 SHENZHEN MEILI MEDICAL DEVICES CO.,LTD come from?
All FDA import refusal data for SHENZHEN MEILI MEDICAL DEVICES 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.