Ardes Zeytinciik Gida Ve Tar. Urun
⚠️ Moderate Risk
FEI: 3010151957 • Umuru-aydin • TURKEY
FEI Number
3010151957
Location
Umuru-aydin
Country
TURKEYAddress
Aydin Organize San Bolgesl, , Umuru-aydin, , 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
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 6/25/2013 | 21GCP09OLIVES (PIT FRUIT) | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 6/25/2013 | 21GCP11OLIVES, GREEN, (PIT FRUIT) | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 6/25/2013 | 21GCP11OLIVES, GREEN, (PIT FRUIT) | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
| 6/25/2013 | 21GGP09OLIVES (PIT FRUIT) | 83NO PROCESS | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Ardes Zeytinciik Gida Ve Tar. Urun's FDA import refusal history?
Ardes Zeytinciik Gida Ve Tar. Urun (FEI: 3010151957) has 4 FDA import refusal record(s) in our database, spanning from 6/25/2013 to 6/25/2013.
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. Ardes Zeytinciik Gida Ve Tar. Urun's FEI number is 3010151957.
What types of violations has Ardes Zeytinciik Gida Ve Tar. Urun received?
Ardes Zeytinciik Gida Ve Tar. Urun 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 Ardes Zeytinciik Gida Ve Tar. Urun come from?
All FDA import refusal data for Ardes Zeytinciik Gida Ve Tar. Urun 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.