Nexos Sac
⚠️ Moderate Risk
FEI: 3009646233 • Lima • PERU
FEI Number
3009646233
Location
Lima
Country
PERUAddress
1 Las Praderas De Santa Anita, , Lima, , 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
PESTICIDE2
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/14/2013 | 24HFH08PEPPER, HOT, DRIED OR PASTE | 3721PESTICIDE2 | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Nexos Sac's FDA import refusal history?
Nexos Sac (FEI: 3009646233) has 1 FDA import refusal record(s) in our database, spanning from 1/14/2013 to 1/14/2013.
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. Nexos Sac's FEI number is 3009646233.
What types of violations has Nexos Sac received?
Nexos Sac has been cited for 1 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 Nexos Sac come from?
All FDA import refusal data for Nexos Sac 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.