P2Life
⚠️ Moderate Risk
FEI: 3012786818 • Cape Town, Western Cape • SOUTH AFRICA
FEI Number
3012786818
Location
Cape Town, Western Cape
Country
SOUTH AFRICAAddress
22 Bell Crescent, , Cape Town, Western Cape, South Africa
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
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 |
|---|---|---|---|
| 8/24/2011 | 54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 11UNSAFE COL | Division of Southeast Imports (DSEI) |
| 8/24/2011 | 54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 11UNSAFE COL | Division of Southeast Imports (DSEI) |
| 8/24/2011 | 54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 11UNSAFE COL | Division of Southeast Imports (DSEI) |
| 8/24/2011 | 54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 11UNSAFE COL | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is P2Life's FDA import refusal history?
P2Life (FEI: 3012786818) has 4 FDA import refusal record(s) in our database, spanning from 8/24/2011 to 8/24/2011.
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. P2Life's FEI number is 3012786818.
What types of violations has P2Life received?
P2Life 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 P2Life come from?
All FDA import refusal data for P2Life 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.