Hd Package
⚠️ Moderate Risk
FEI: 3010279364 • Dukyang • SOUTH KOREA
FEI Number
3010279364
Location
Dukyang
Country
SOUTH KOREAAddress
231-36 Naeyoung, Koyang-See, Dukyang, , 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
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 ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/9/2014 | 89KNMDEVICE, PRESSURE APPLYING | Los Angeles District Office (LOS-DO) | |
| 1/9/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 3260NO ENGLISH | Los Angeles District Office (LOS-DO) |
| 1/7/2014 | 79LRRKIT, FIRST AID | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 1/6/2014 | 79LRRKIT, FIRST AID | 341REGISTERED | Los Angeles District Office (LOS-DO) |
| 1/6/2014 | 79LRRKIT, FIRST AID | 341REGISTERED | Los Angeles District Office (LOS-DO) |
| 1/6/2014 | 79LRRKIT, FIRST AID | 341REGISTERED | Los Angeles District Office (LOS-DO) |
| 1/6/2014 | 79LRRKIT, FIRST AID | 341REGISTERED | Los Angeles District Office (LOS-DO) |
| 1/6/2014 | 79LRRKIT, FIRST AID | 341REGISTERED | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Hd Package's FDA import refusal history?
Hd Package (FEI: 3010279364) has 8 FDA import refusal record(s) in our database, spanning from 1/6/2014 to 1/9/2014.
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. Hd Package's FEI number is 3010279364.
What types of violations has Hd Package received?
Hd Package 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 Hd Package come from?
All FDA import refusal data for Hd Package 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.