Pro-Life Imp.
⚠️ Moderate Risk
FEI: 3004902595 • Sao Paulo • BRAZIL
FEI Number
3004902595
Location
Sao Paulo
Country
BRAZILAddress
02.989.746/0001-03, , 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.
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.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/17/2005 | 53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | 11UNSAFE COL | New Orleans District Office (NOL-DO) |
| 2/15/2005 | 53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | New Orleans District Office (NOL-DO) | |
| 2/15/2005 | 53YY99OTHER COSMETIC AND COSMETIC PRODUCTS, N.E.C. | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Pro-Life Imp.'s FDA import refusal history?
Pro-Life Imp. (FEI: 3004902595) has 3 FDA import refusal record(s) in our database, spanning from 2/15/2005 to 2/17/2005.
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. Pro-Life Imp.'s FEI number is 3004902595.
What types of violations has Pro-Life Imp. received?
Pro-Life Imp. has been cited for 3 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 Pro-Life Imp. come from?
All FDA import refusal data for Pro-Life Imp. 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.