Satori Sol Inc
✅ Low Risk
FEI: 3004593151 • Phoenix, AZ • UNITED STATES
FEI Number
3004593151
Location
Phoenix, AZ
Country
UNITED STATESAddress
17209 Noth 41st, , Phoenix, AZ, United States
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
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.
COSMETLBLG
It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.
Refusal History
Frequently Asked Questions
What is Satori Sol Inc's FDA import refusal history?
Satori Sol Inc (FEI: 3004593151) has 1 FDA import refusal record(s) in our database, spanning from 8/23/2004 to 8/23/2004.
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. Satori Sol Inc's FEI number is 3004593151.
What types of violations has Satori Sol Inc received?
Satori Sol Inc has been cited for 2 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 Satori Sol Inc come from?
All FDA import refusal data for Satori Sol Inc 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.