Imv Equipements D'Insemination Artificielle Et D'Elevage
⚠️ Moderate Risk
FEI: 1000597707 • L Aigle CEDEX • FRANCE
FEI Number
1000597707
Location
L Aigle CEDEX
Country
FRANCEAddress
10 Rue Clemenceau, , L Aigle CEDEX, , France
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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/18/2002 | 68YYY20ANIMAL DRUGS N.E.C. USED MORE THAN 1 SPECIES | 118NOT LISTED | Minneapolis District Office (MIN-DO) |
| 3/18/2002 | 68YYY20ANIMAL DRUGS N.E.C. USED MORE THAN 1 SPECIES | 118NOT LISTED | Minneapolis District Office (MIN-DO) |
| 3/18/2002 | 68YYY20ANIMAL DRUGS N.E.C. USED MORE THAN 1 SPECIES | 118NOT LISTED | Minneapolis District Office (MIN-DO) |
Frequently Asked Questions
What is Imv Equipements D'Insemination Artificielle Et D'Elevage's FDA import refusal history?
Imv Equipements D'Insemination Artificielle Et D'Elevage (FEI: 1000597707) has 3 FDA import refusal record(s) in our database, spanning from 3/18/2002 to 3/18/2002.
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. Imv Equipements D'Insemination Artificielle Et D'Elevage's FEI number is 1000597707.
What types of violations has Imv Equipements D'Insemination Artificielle Et D'Elevage received?
Imv Equipements D'Insemination Artificielle Et D'Elevage 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 Imv Equipements D'Insemination Artificielle Et D'Elevage come from?
All FDA import refusal data for Imv Equipements D'Insemination Artificielle Et D'Elevage 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.