South Am Freeze Dry
⚠️ High Risk
FEI: 3009931169 • Viluco-buin, CL-RM • CHILE
FEI Number
3009931169
Location
Viluco-buin, CL-RM
Country
CHILEAddress
Las Vertientes No. 2589, Santa Filomena, Viluco-buin, CL-RM, Chile
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
Frequently Asked Questions
What is South Am Freeze Dry's FDA import refusal history?
South Am Freeze Dry (FEI: 3009931169) has 2 FDA import refusal record(s) in our database, spanning from 12/21/2022 to 7/8/2025.
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. South Am Freeze Dry's FEI number is 3009931169.
What types of violations has South Am Freeze Dry received?
South Am Freeze Dry 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 South Am Freeze Dry come from?
All FDA import refusal data for South Am Freeze Dry 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.