SoliPharma B.V.
⚠️ Moderate Risk
FEI: 3013167880 • Oudenbosch, Noord-Brabant • NETHERLANDS
FEI Number
3013167880
Location
Oudenbosch, Noord-Brabant
Country
NETHERLANDSAddress
And 11a, Industrieweg 17, Oudenbosch, Noord-Brabant, Netherlands
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
UNSFDIETSP
The article appears to be a dietary supplement or ingredient for which there is inadequate information to provide reasonable assurance that such ingredient does not present a significant or unreasonable risk of illness or injury.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/5/2014 | 54ABE99VITAMIN, N.E.C. | 2120UNSFDIETSP | Division of Southeast Imports (DSEI) |
| 9/5/2014 | 54ABE99VITAMIN, N.E.C. | 2120UNSFDIETSP | New Orleans District Office (NOL-DO) |
| 9/5/2014 | 54ABE99VITAMIN, N.E.C. | 2120UNSFDIETSP | New Orleans District Office (NOL-DO) |
| 8/20/2014 | 54YBY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C. | 2120UNSFDIETSP | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is SoliPharma B.V.'s FDA import refusal history?
SoliPharma B.V. (FEI: 3013167880) has 4 FDA import refusal record(s) in our database, spanning from 8/20/2014 to 9/5/2014.
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. SoliPharma B.V.'s FEI number is 3013167880.
What types of violations has SoliPharma B.V. received?
SoliPharma B.V. 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 SoliPharma B.V. come from?
All FDA import refusal data for SoliPharma B.V. 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.