CELLRETURN CO LTD
⚠️ Moderate Risk
FEI: 3015959898 • Incheon • SOUTH KOREA
FEI Number
3015959898
Location
Incheon
Country
SOUTH KOREAAddress
237 Namdongseo-Ro Namdo, , Incheon, , South Korea
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 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.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/28/2022 | 79OHSLIGHT BASED OVER THE COUNTER WRINKLE REDUCTION | Division of Southeast Imports (DSEI) | |
| 8/13/2021 | 79OLPOVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE | Division of Southeast Imports (DSEI) | |
| 7/13/2021 | 79OLPOVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE | Division of Southeast Imports (DSEI) | |
| 12/31/2020 | 79OLPOVER-THE-COUNTER POWERED RED/BLUE LIGHT BASED LASER FOR ACNE | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is CELLRETURN CO LTD's FDA import refusal history?
CELLRETURN CO LTD (FEI: 3015959898) has 4 FDA import refusal record(s) in our database, spanning from 12/31/2020 to 4/28/2022.
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. CELLRETURN CO LTD's FEI number is 3015959898.
What types of violations has CELLRETURN CO LTD received?
CELLRETURN CO LTD 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 CELLRETURN CO LTD come from?
All FDA import refusal data for CELLRETURN 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.