Min Gida
⚠️ Moderate Risk
FEI: 3003491601 • Ankara, Ankara • TURKEY
FEI Number
3003491601
Location
Ankara, Ankara
Country
TURKEYAddress
Strazburg C, , Ankara, Ankara, 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
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
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 |
|---|---|---|---|
| 10/6/2004 | 25ECI99MIXED VEGETABLES, N.E.C. | New York District Office (NYK-DO) | |
| 10/6/2004 | 24TCI08CABBAGE (LEAF & STEM VEGETABLE) | New York District Office (NYK-DO) | |
| 10/6/2004 | 24FCI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Min Gida's FDA import refusal history?
Min Gida (FEI: 3003491601) has 3 FDA import refusal record(s) in our database, spanning from 10/6/2004 to 10/6/2004.
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. Min Gida's FEI number is 3003491601.
What types of violations has Min Gida received?
Min Gida 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 Min Gida come from?
All FDA import refusal data for Min Gida 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.