Hk Glm Beauty Spa Equipment
⚠️ Moderate Risk
FEI: 3008644894 • Baiyun • CHINA
FEI Number
3008644894
Location
Baiyun
Country
CHINAAddress
4th Floor B Building 1st District Rongxi, , Baiyun, , 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).
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.
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).
NON STD
The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/21/2011 | 95RDWGENERAL PURPOSE LASER PRODUCTS, NON-MEDICAL | Los Angeles District Office (LOS-DO) | |
| 6/14/2011 | 89LXFDIATHERMY, ULTRASONIC, FOR USE OTHER THAN APPLYING THERAPEUTIC DEEP HEAT | Cincinnati District Office (CIN-DO) | |
| 12/28/2010 | 89LBFDEVICE, THERAPY, DIRECT CURRENT, LOW INTENSITY | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is Hk Glm Beauty Spa Equipment's FDA import refusal history?
Hk Glm Beauty Spa Equipment (FEI: 3008644894) has 3 FDA import refusal record(s) in our database, spanning from 12/28/2010 to 7/21/2011.
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. Hk Glm Beauty Spa Equipment's FEI number is 3008644894.
What types of violations has Hk Glm Beauty Spa Equipment received?
Hk Glm Beauty Spa Equipment has been cited for 6 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 Hk Glm Beauty Spa Equipment come from?
All FDA import refusal data for Hk Glm Beauty Spa Equipment 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.