New Age
⚠️ Moderate Risk
FEI: 3011091020 • Lugo, Ravenna • ITALY
FEI Number
3011091020
Location
Lugo, Ravenna
Country
ITALYAddress
Viale De' Brozzi 3, , Lugo, Ravenna, 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
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).
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/11/2018 | 86ORSMAGNETOTHERAPY DEVICE FOR PAIN RELIEF | Division of Southeast Imports (DSEI) | |
| 4/11/2018 | 86ORSMAGNETOTHERAPY DEVICE FOR PAIN RELIEF | Division of Southeast Imports (DSEI) | |
| 11/10/2014 | 86ORSMAGNETOTHERAPY DEVICE FOR PAIN RELIEF | Cincinnati District Office (CIN-DO) |
Frequently Asked Questions
What is New Age's FDA import refusal history?
New Age (FEI: 3011091020) has 3 FDA import refusal record(s) in our database, spanning from 11/10/2014 to 4/11/2018.
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. New Age's FEI number is 3011091020.
What types of violations has New Age received?
New Age has been cited for 4 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 New Age come from?
All FDA import refusal data for New Age 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.