Alterra S.A.
⚠️ Moderate Risk
FEI: 3005204525 • Giannitsa • GREECE
FEI Number
3005204525
Location
Giannitsa
Country
GREECEAddress
3rd Km Giannitsa-Edessa, , Giannitsa, , Greece
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
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:
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/2/2019 | 24TGD25SPINACH (LEAF & STEM VEGETABLE) | 238UNSAFE ADD | Division of Northeast Imports (DNEI) |
| 1/28/2014 | 21GGD03CHERRY FRUIT (PIT FRUIT) | 241PESTICIDE | Seattle District Office (SEA-DO) |
| 1/14/2014 | 21GGD03CHERRY FRUIT (PIT FRUIT) | 241PESTICIDE | Seattle District Office (SEA-DO) |
| 12/18/2013 | 21GGD03CHERRY FRUIT (PIT FRUIT) | 241PESTICIDE | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Alterra S.A.'s FDA import refusal history?
Alterra S.A. (FEI: 3005204525) has 4 FDA import refusal record(s) in our database, spanning from 12/18/2013 to 8/2/2019.
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. Alterra S.A.'s FEI number is 3005204525.
What types of violations has Alterra S.A. received?
Alterra S.A. has been cited for 2 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 Alterra S.A. come from?
All FDA import refusal data for Alterra S.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.