Shenzhen Anpan Health Industry Co., Ltd
⚠️ Moderate Risk
FEI: 3006278725 • Shenzhen, Guangdong • CHINA
FEI Number
3006278725
Location
Shenzhen, Guangdong
Country
CHINAAddress
No 44 -46 Xiakeng Road, Longgangjiedao Longgang, 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).
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/5/2016 | 89IRTPAD, HEATING, POWERED | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 1/27/2015 | 89LBGDEVICE, FLUIDIZED THERAPY, DRY HEAT | Los Angeles District Office (LOS-DO) | |
| 1/27/2015 | 89LBGDEVICE, FLUIDIZED THERAPY, DRY HEAT | Los Angeles District Office (LOS-DO) | |
| 1/27/2015 | 89LBGDEVICE, FLUIDIZED THERAPY, DRY HEAT | Los Angeles District Office (LOS-DO) | |
| 1/27/2015 | 89LBGDEVICE, FLUIDIZED THERAPY, DRY HEAT | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Shenzhen Anpan Health Industry Co., Ltd's FDA import refusal history?
Shenzhen Anpan Health Industry Co., Ltd (FEI: 3006278725) has 5 FDA import refusal record(s) in our database, spanning from 1/27/2015 to 5/5/2016.
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 Anpan Health Industry Co., Ltd's FEI number is 3006278725.
What types of violations has Shenzhen Anpan Health Industry Co., Ltd received?
Shenzhen Anpan Health Industry Co., Ltd has been cited for 4 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 Anpan Health Industry Co., Ltd come from?
All FDA import refusal data for Shenzhen Anpan Health Industry 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.