SE FACTORY
⚠️ Moderate Risk
FEI: 3019817799 • Groningen, Groningen • NETHERLANDS
FEI Number
3019817799
Location
Groningen, Groningen
Country
NETHERLANDSAddress
Zernikepark 12, , Groningen, Groningen, Netherlands
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.
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/PDP
The article appears to be a class III dev.w/o an approved applic. for premarket approval, and/or a notice of completion of product development protocol filed per section 515(b) or exempt per sect.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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/6/2023 | 89NHNLAMP, NON-HEATING, FOR ADJUNCTIVE USE IN PAIN THERAPY | Division of Southeast Imports (DSEI) | |
| 11/6/2023 | 89NHNLAMP, NON-HEATING, FOR ADJUNCTIVE USE IN PAIN THERAPY | Division of Southeast Imports (DSEI) | |
| 11/6/2023 | 84PWECOGNITIVE BEHAVIORAL THERAPY DEVICE FOR PSYCHIATRIC DISORDERS | Division of Southeast Imports (DSEI) | |
| 3/23/2022 | 84PWECOGNITIVE BEHAVIORAL THERAPY DEVICE FOR PSYCHIATRIC DISORDERS | Division of Southeast Imports (DSEI) | |
| 12/23/2021 | 86HLLMONITOR, EYE MOVEMENT | Division of Southeast Imports (DSEI) | |
| 12/8/2021 | 84PWECOGNITIVE BEHAVIORAL THERAPY DEVICE FOR PSYCHIATRIC DISORDERS | Division of Southeast Imports (DSEI) | |
| 11/30/2021 | 79MYHSYSTEM, NON-COHERENT LIGHT, PHOTODYNAMIC THERAPY | Division of Southeast Imports (DSEI) | |
| 10/15/2021 | 84PWECOGNITIVE BEHAVIORAL THERAPY DEVICE FOR PSYCHIATRIC DISORDERS | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is SE FACTORY's FDA import refusal history?
SE FACTORY (FEI: 3019817799) has 8 FDA import refusal record(s) in our database, spanning from 10/15/2021 to 12/6/2023.
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. SE FACTORY's FEI number is 3019817799.
What types of violations has SE FACTORY received?
SE FACTORY has been cited for 5 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 SE FACTORY come from?
All FDA import refusal data for SE FACTORY 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.