Sterling S.p.A
⚠️ Moderate Risk
FEI: 3003042159 • Corciano, Perugia • ITALY
FEI Number
3003042159
Location
Corciano, Perugia
Country
ITALYAddress
Solomeo, Via Della Carboneria 30/32, Corciano, Perugia, 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).
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).
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
INSANITARY
The article is subject to refusal of admission pursuant to section 801(a)(3) in that the article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth, or whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/2/2017 | 64LCS99GLUCOCORTICOID N.E.C. | New Orleans District Office (NOL-DO) | |
| 6/11/2015 | 61ECS04BUDESONIDE (ANTI-ASTHMATIC) | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/2/2014 | 61ECS04BUDESONIDE (ANTI-ASTHMATIC) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 11/7/2013 | 61UIZ07FULVESTRANT | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Sterling S.p.A's FDA import refusal history?
Sterling S.p.A (FEI: 3003042159) has 4 FDA import refusal record(s) in our database, spanning from 11/7/2013 to 2/2/2017.
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. Sterling S.p.A's FEI number is 3003042159.
What types of violations has Sterling S.p.A received?
Sterling S.p.A 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 Sterling S.p.A come from?
All FDA import refusal data for Sterling S.p.A 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.