VESTA TARIM URUNLERI A.S.
⚠️ Moderate Risk
FEI: 3005360525 • Malatya, Malatya • TURKEY
FEI Number
3005360525
Location
Malatya, Malatya
Country
TURKEYAddress
Mevkii Cumhuriyet Ornekkoy Onatli, , Malatya, Malatya, Turkey
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
PESTICIDES
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
Frequently Asked Questions
What is VESTA TARIM URUNLERI A.S.'s FDA import refusal history?
VESTA TARIM URUNLERI A.S. (FEI: 3005360525) has 2 FDA import refusal record(s) in our database, spanning from 3/14/2005 to 3/14/2005.
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. VESTA TARIM URUNLERI A.S.'s FEI number is 3005360525.
What types of violations has VESTA TARIM URUNLERI A.S. received?
VESTA TARIM URUNLERI A.S. 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 VESTA TARIM URUNLERI A.S. come from?
All FDA import refusal data for VESTA TARIM URUNLERI A.S. 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.