Erica Akemi Murakami-Me
⚠️ Moderate Risk
FEI: 3011254219 • Sao Paulo • BRAZIL
FEI Number
3011254219
Location
Sao Paulo
Country
BRAZILAddress
Rua Antonio Paulista 293, , Sao Paulo, , Brazil
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
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/15/2016 | 53DY99OTHER FRAGRANCE PREPARATIONS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 4/15/2016 | 53DY99OTHER FRAGRANCE PREPARATIONS, N.E.C. | Division of Northeast Imports (DNEI) | |
| 11/19/2015 | 53JA02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | 471CSTIC LBLG | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Erica Akemi Murakami-Me's FDA import refusal history?
Erica Akemi Murakami-Me (FEI: 3011254219) has 3 FDA import refusal record(s) in our database, spanning from 11/19/2015 to 4/15/2016.
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. Erica Akemi Murakami-Me's FEI number is 3011254219.
What types of violations has Erica Akemi Murakami-Me received?
Erica Akemi Murakami-Me has been cited for 4 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 Erica Akemi Murakami-Me come from?
All FDA import refusal data for Erica Akemi Murakami-Me 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.