MIKO Co., Ltd.
⚠️ Moderate Risk
FEI: 3019027389 • Pohang, Gyeongsangbuk • SOUTH KOREA
FEI Number
3019027389
Location
Pohang, Gyeongsangbuk
Country
SOUTH KOREAAddress
110 Chilpo-Ro, Buk, Pohang, Gyeongsangbuk, 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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/8/2022 | 63RAK04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC) | 118NOT LISTED | Division of West Coast Imports (DWCI) |
| 11/8/2022 | 63RAK04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC) | 118NOT LISTED | Division of West Coast Imports (DWCI) |
| 11/8/2022 | 63RAK04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC) | 118NOT LISTED | Division of West Coast Imports (DWCI) |
| 11/8/2022 | 63RAK04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC) | 118NOT LISTED | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is MIKO Co., Ltd.'s FDA import refusal history?
MIKO Co., Ltd. (FEI: 3019027389) has 4 FDA import refusal record(s) in our database, spanning from 11/8/2022 to 11/8/2022.
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. MIKO Co., Ltd.'s FEI number is 3019027389.
What types of violations has MIKO Co., Ltd. received?
MIKO Co., Ltd. has been cited for 1 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 MIKO Co., Ltd. come from?
All FDA import refusal data for MIKO 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.