KAIWEI SHENZHEN CO LTD
✅ Low Risk
FEI: 3014400630 • Shenzhen • CHINA
FEI Number
3014400630
Location
Shenzhen
Country
CHINAAddress
5f Zhihai Industry Park, , Shenzhen, , 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).
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.
Refusal History
Frequently Asked Questions
What is KAIWEI SHENZHEN CO LTD's FDA import refusal history?
KAIWEI SHENZHEN CO LTD (FEI: 3014400630) has 1 FDA import refusal record(s) in our database, spanning from 5/26/2020 to 5/26/2020.
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. KAIWEI SHENZHEN CO LTD's FEI number is 3014400630.
What types of violations has KAIWEI SHENZHEN CO LTD received?
KAIWEI SHENZHEN 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 KAIWEI SHENZHEN CO LTD come from?
All FDA import refusal data for KAIWEI SHENZHEN 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.