Kyungwon Medical Co., Ltd.
⚠️ Moderate Risk
FEI: 3006455376 • Osong-eup, Chungcheongbuk-do • SOUTH KOREA
FEI Number
3006455376
Location
Osong-eup, Chungcheongbuk-do
Country
SOUTH KOREAAddress
765, Jeongjungyeonje-ro, , Osong-eup, Chungcheongbuk-do, 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
DEVICEGMPS
The article is subject to refusal of admission pursuant to Section 801(a)(1) in that the methods used in, or the facilities or controls used for, the manufacture, packing, storage, or installation of the device do not conform to the requirements of Section 520(f)(1) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) or a condition prescribed by an order under section 520(f)(2) of the FD&C 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).
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/11/2016 | 87MQVFILLER, CALCIUM SULFATE PREFORMED PELLETS | Seattle District Office (SEA-DO) | |
| 2/15/2013 | 87MQVFILLER, CALCIUM SULFATE PREFORMED PELLETS | Seattle District Office (SEA-DO) | |
| 2/15/2013 | 84GXPMETHYL METACRYLATE FOR CRANIOPLASTY | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Kyungwon Medical Co., Ltd.'s FDA import refusal history?
Kyungwon Medical Co., Ltd. (FEI: 3006455376) has 3 FDA import refusal record(s) in our database, spanning from 2/15/2013 to 1/11/2016.
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. Kyungwon Medical Co., Ltd.'s FEI number is 3006455376.
What types of violations has Kyungwon Medical Co., Ltd. received?
Kyungwon Medical Co., Ltd. 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 Kyungwon Medical Co., Ltd. come from?
All FDA import refusal data for Kyungwon Medical 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.