Lanxess Deutchland Gmbh
⚠️ Moderate Risk
FEI: 3010850251 • Krefeld • GERMANY
FEI Number
3010850251
Location
Krefeld
Country
GERMANYAddress
Bu Ruc-P&T-Znobuilding R 10, , Krefeld, , 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
UNFIT4FOOD
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be unfit for food.
COLORLABEL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use.
Refusal History
Frequently Asked Questions
What is Lanxess Deutchland Gmbh's FDA import refusal history?
Lanxess Deutchland Gmbh (FEI: 3010850251) has 2 FDA import refusal record(s) in our database, spanning from 2/11/2016 to 2/11/2016.
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. Lanxess Deutchland Gmbh's FEI number is 3010850251.
What types of violations has Lanxess Deutchland Gmbh received?
Lanxess Deutchland 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 Lanxess Deutchland Gmbh come from?
All FDA import refusal data for Lanxess Deutchland 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.