Dr Hobein Gmbh
⚠️ Moderate Risk
FEI: 3005293941 • Meckenheim • GERMANY
FEI Number
3005293941
Location
Meckenheim
Country
GERMANYAddress
Medizinlsche Hautpflege Grezstra, , Meckenheim, , Germany
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.
HEALTH C
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/19/2012 | 53LD99OTHER SKIN CARE PREPARATIONS, N.E.C. | 471CSTIC LBLG | New Orleans District Office (NOL-DO) |
| 6/19/2012 | 53LD99OTHER SKIN CARE PREPARATIONS, N.E.C. | 471CSTIC LBLG | New Orleans District Office (NOL-DO) |
| 6/21/2007 | 54GDM99ANIMAL BY-PRODUCTS AND EXTRACTS, N.E.C. | 488HEALTH C | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Dr Hobein Gmbh's FDA import refusal history?
Dr Hobein Gmbh (FEI: 3005293941) has 3 FDA import refusal record(s) in our database, spanning from 6/21/2007 to 6/19/2012.
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. Dr Hobein Gmbh's FEI number is 3005293941.
What types of violations has Dr Hobein Gmbh received?
Dr Hobein Gmbh has been cited for 2 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 Dr Hobein Gmbh come from?
All FDA import refusal data for Dr Hobein Gmbh 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.