Epitech Group
⚠️ Moderate Risk
FEI: 3006167824 • Milan, Milan • ITALY
FEI Number
3006167824
Location
Milan, Milan
Country
ITALYAddress
Via Egadi 7, , Milan, Milan, Italy
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
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).
INCONSPICU
Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/24/2018 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 5/29/2018 | 66VBE99MISCELLANEOUS PATENT MEDICINES, ETC. | 336INCONSPICU | Division of Northern Border Imports (DNBI) |
| 3/4/2013 | 60LAY99ANALGESIC, N.E.C. | Philadelphia District Office (PHI-DO) |
Frequently Asked Questions
What is Epitech Group's FDA import refusal history?
Epitech Group (FEI: 3006167824) has 3 FDA import refusal record(s) in our database, spanning from 3/4/2013 to 8/24/2018.
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. Epitech Group's FEI number is 3006167824.
What types of violations has Epitech Group received?
Epitech Group 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 Epitech Group come from?
All FDA import refusal data for Epitech Group 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.