Wehling Prof Praxis
✅ Low Risk
FEI: 3005306878 • Duesseldorf • GERMANY
FEI Number
3005306878
Location
Duesseldorf
Country
GERMANYAddress
Roenistr 55 Il, , Duesseldorf, , Germany
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.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
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 |
|---|---|---|---|
| 3/15/2007 | 53LC03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS) | New Orleans District Office (NOL-DO) | |
| 2/16/2007 | 61GDB34ROSAMICIN STEARATE (ANTI-BACTERIAL) (NOT ANTIBIOTIC) | 472NO ENGLISH | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Wehling Prof Praxis's FDA import refusal history?
Wehling Prof Praxis (FEI: 3005306878) has 2 FDA import refusal record(s) in our database, spanning from 2/16/2007 to 3/15/2007.
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. Wehling Prof Praxis's FEI number is 3005306878.
What types of violations has Wehling Prof Praxis received?
Wehling Prof Praxis 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 Wehling Prof Praxis come from?
All FDA import refusal data for Wehling Prof Praxis 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.