AG CO LTD
⚠️ Moderate Risk
FEI: 3013851849 • Chungju • SOUTH KOREA
FEI Number
3013851849
Location
Chungju
Country
SOUTH KOREAAddress
40 Megapolis-Ro Daesowo, , Chungju, , 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
COSM COLOR
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
LACKS FIRM
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
COLOR LBLG
The color additive appears to not have its packaging and labeling in conformity with such requirements as issued under section 721.
COSM MISB2
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears that its labeling is false or misleading in any particular.
COSMETFPLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an undeclared color additive which renders it misbranded within the meaning of Sections 1454(c)(3)(B) and 1456 of the Fair Packaging and Labeling Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/20/2020 | 53CD14EYELASH AND EYEBROW TREATMENTS-GEL, OIL, PRIMER, CONDITIONERS, SERUM, FORTIFIERS (EYE MAKEUP PREPARA | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 10/20/2020 | 53CD06MASCARA (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 10/20/2020 | 53CD06MASCARA (EYE MAKEUP PREPARATIONS) | 320LACKS FIRM | Division of Southeast Imports (DSEI) |
| 10/20/2020 | 53CD13EYELASH AND EYEBROW ADHESIVE (EYE MAKEUP PREPARATIONS) | Division of Southeast Imports (DSEI) | |
| 4/9/2019 | 53CD13EYELASH AND EYEBROW ADHESIVE (EYE MAKEUP PREPARATIONS) | 471CSTIC LBLG | Division of Southeast Imports (DSEI) |
| 12/4/2018 | 53CD13EYELASH AND EYEBROW ADHESIVE (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Division of Northern Border Imports (DNBI) |
| 12/4/2018 | 53CD13EYELASH AND EYEBROW ADHESIVE (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Division of Northern Border Imports (DNBI) |
| 11/29/2018 | 53CY13EYELASH AND EYEBROW ADHESIVE (EYE MAKEUP PREPARATIONS) | 197COSM COLOR | Division of Northern Border Imports (DNBI) |
| 10/22/2018 | 53CY99OTHER EYE MAKEUP PREPARATIONS, N.E.C. | 197COSM COLOR | Division of Southeast Imports (DSEI) |
| 12/13/2017 | 53CD08EYE MAKEUP KITS (EYE MAKEUP PREPARATIONS) | 198COLOR LBLG | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is AG CO LTD's FDA import refusal history?
AG CO LTD (FEI: 3013851849) has 10 FDA import refusal record(s) in our database, spanning from 12/13/2017 to 10/20/2020.
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. AG CO LTD's FEI number is 3013851849.
What types of violations has AG CO LTD received?
AG CO LTD has been cited for 6 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 AG CO LTD come from?
All FDA import refusal data for AG 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.