SHENZHEN XITANG INTERNATIONAL TRADI
⚠️ Moderate Risk
FEI: 3016704444 • Shenzhen, Guangdong • CHINA
FEI Number
3016704444
Location
Shenzhen, Guangdong
Country
CHINAAddress
2008 Taibangkejidasha,Nanshankejiyuan,Nanshan Dis, , Shenzhen, 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
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.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/3/2024 | 86NJHLENS, SPECTACLE (PRESCRIPTION), FOR READING DISCOMFORT | 341REGISTERED | Division of West Coast Imports (DWCI) |
| 11/30/2023 | 86HQGLENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION) | 3280FRNMFGREG | Division of Southwest Imports (DSWI) |
| 10/15/2023 | 86NJHLENS, SPECTACLE (PRESCRIPTION), FOR READING DISCOMFORT | 341REGISTERED | Division of West Coast Imports (DWCI) |
| 1/8/2021 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | Division of Southeast Imports (DSEI) | |
| 11/18/2020 | 86HQZFRAME, SPECTACLE | Division of Southeast Imports (DSEI) | |
| 11/10/2020 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | 3280FRNMFGREG | Division of Southeast Imports (DSEI) |
| 11/6/2020 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | Division of Southeast Imports (DSEI) | |
| 10/30/2020 | 86HQZFRAME, SPECTACLE | Division of West Coast Imports (DWCI) | |
| 10/30/2020 | 86HQZFRAME, SPECTACLE | Division of Southeast Imports (DSEI) | |
| 10/22/2020 | 86HQYSUNGLASSES (NON-PRESCRIPTION INCLUDING PHOTOSENSITIVE) | Division of West Coast Imports (DWCI) | |
| 10/22/2020 | 86HQZFRAME, SPECTACLE | 118NOT LISTED | Division of West Coast Imports (DWCI) |
| 10/19/2020 | 86HQZFRAME, SPECTACLE | 118NOT LISTED | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is SHENZHEN XITANG INTERNATIONAL TRADI's FDA import refusal history?
SHENZHEN XITANG INTERNATIONAL TRADI (FEI: 3016704444) has 12 FDA import refusal record(s) in our database, spanning from 10/19/2020 to 1/3/2024.
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 XITANG INTERNATIONAL TRADI's FEI number is 3016704444.
What types of violations has SHENZHEN XITANG INTERNATIONAL TRADI received?
SHENZHEN XITANG INTERNATIONAL TRADI 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 SHENZHEN XITANG INTERNATIONAL TRADI come from?
All FDA import refusal data for SHENZHEN XITANG INTERNATIONAL TRADI 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.