Ellis Toussier
⚠️ Moderate Risk
FEI: 3003256135 • Ciudad De Mexico, Ciudad de Mexico • MEXICO
FEI Number
3003256135
Location
Ciudad De Mexico, Ciudad de Mexico
Country
MEXICOAddress
Avenida Horacio 1729-5, Col. Polanco I Seccion, Miguel Hidalgo, Ciudad De Mexico, Ciudad de Mexico, Mexico
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).
AGR RX
The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/21/2002 | 77KBRNEEDLE, TONSIL SUTURING | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 6/7/2002 | 80LDQDEVICE, GENERAL MEDICAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 4/10/2002 | 66VAY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 1/6/2002 | 61FDA54CIPROFLOXACIN (ANTI-BACTERIAL PART I) (NOT ANTIBIOTIC) | 179AGR RX | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Ellis Toussier's FDA import refusal history?
Ellis Toussier (FEI: 3003256135) has 4 FDA import refusal record(s) in our database, spanning from 1/6/2002 to 8/21/2002.
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. Ellis Toussier's FEI number is 3003256135.
What types of violations has Ellis Toussier received?
Ellis Toussier 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 Ellis Toussier come from?
All FDA import refusal data for Ellis Toussier 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.