AMORE PACIFIC
⚠️ Moderate Risk
FEI: 3016611615 • Korea • SOUTH KOREA
FEI Number
3016611615
Location
Korea
Country
SOUTH KOREAAddress
Osan, Gyeonggi-Do 18103, , Korea, , 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).
DRUG GMPS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the methods used in and controls used for the manufacture, processing, packing, or holding of drugs and other products do not appear to conform to current good manufacturing practices within the meaning of Section 501(a)(2)(B).
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 |
|---|---|---|---|
| 8/8/2023 | 66PBL18ZINC OXIDE (ULTRAVIOLET SCREEN/SUNSCREEN) | 118NOT LISTED | Division of Northeast Imports (DNEI) |
| 8/8/2023 | 66PBL18ZINC OXIDE (ULTRAVIOLET SCREEN/SUNSCREEN) | 118NOT LISTED | Division of Northeast Imports (DNEI) |
| 7/27/2023 | 66PBL18ZINC OXIDE (ULTRAVIOLET SCREEN/SUNSCREEN) | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is AMORE PACIFIC's FDA import refusal history?
AMORE PACIFIC (FEI: 3016611615) has 3 FDA import refusal record(s) in our database, spanning from 7/27/2023 to 8/8/2023.
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. AMORE PACIFIC's FEI number is 3016611615.
What types of violations has AMORE PACIFIC received?
AMORE PACIFIC 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 AMORE PACIFIC come from?
All FDA import refusal data for AMORE PACIFIC 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.