Pacific Segwang Co
✅ Low Risk
FEI: 3007559155 • Gyeonggi-do • SOUTH KOREA
FEI Number
3007559155
Location
Gyeonggi-do
Country
SOUTH KOREAAddress
382-6 Galmae-Dong, Guri-Si, , Gyeonggi-do, , South Korea
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/3/2009 | 76NREMECHANICAL TOOTH DESENSITIZER IN TOOTHPASTE | 3260NO ENGLISH | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Pacific Segwang Co's FDA import refusal history?
Pacific Segwang Co (FEI: 3007559155) has 1 FDA import refusal record(s) in our database, spanning from 9/3/2009 to 9/3/2009.
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. Pacific Segwang Co's FEI number is 3007559155.
What types of violations has Pacific Segwang Co received?
Pacific Segwang Co 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 Pacific Segwang Co come from?
All FDA import refusal data for Pacific Segwang Co 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.