SANOFIL AVENTIS DEL PERU SA
⚠️ Moderate Risk
FEI: 3015010211 • San Isidro, Huaytara • PERU
FEI Number
3015010211
Location
San Isidro, Huaytara
Country
PERUAddress
Calle Los Sauces 374, , San Isidro, Huaytara, Peru
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).
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.
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
Frequently Asked Questions
What is SANOFIL AVENTIS DEL PERU SA's FDA import refusal history?
SANOFIL AVENTIS DEL PERU SA (FEI: 3015010211) has 1 FDA import refusal record(s) in our database, spanning from 11/21/2023 to 11/21/2023.
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. SANOFIL AVENTIS DEL PERU SA's FEI number is 3015010211.
What types of violations has SANOFIL AVENTIS DEL PERU SA received?
SANOFIL AVENTIS DEL PERU SA 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 SANOFIL AVENTIS DEL PERU SA come from?
All FDA import refusal data for SANOFIL AVENTIS DEL PERU SA 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.