BOEHRINGER INGELHEIM FOR NOVO NO
⚠️ High Risk
FEI: 3014882649 • Bagsvard, Hovedstaden • DENMARK
FEI Number
3014882649
Location
Bagsvard, Hovedstaden
Country
DENMARKAddress
Novo Alle 1, , Bagsvard, Hovedstaden, Denmark
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable 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
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
Refusal History
Frequently Asked Questions
What is BOEHRINGER INGELHEIM FOR NOVO NO's FDA import refusal history?
BOEHRINGER INGELHEIM FOR NOVO NO (FEI: 3014882649) has 3 FDA import refusal record(s) in our database, spanning from 7/2/2025 to 10/14/2025.
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. BOEHRINGER INGELHEIM FOR NOVO NO's FEI number is 3014882649.
What types of violations has BOEHRINGER INGELHEIM FOR NOVO NO received?
BOEHRINGER INGELHEIM FOR NOVO NO has been cited for 3 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 BOEHRINGER INGELHEIM FOR NOVO NO come from?
All FDA import refusal data for BOEHRINGER INGELHEIM FOR NOVO NO 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.