D. VOURDERIS & CO O.E.E.
⚠️ Moderate Risk
FEI: 3004293972 • AEGION, ACHAIA • GREECE
FEI Number
3004293972
Location
AEGION, ACHAIA
Country
GREECEAddress
NIKOLEIKA AEGION, , AEGION, ACHAIA, 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
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).
SULFITELBL
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded because 1) it appears to contain sulfites but the label fails to declare the presence of sulfites, a fact material to sulfite-sensitive individuals who must avoid the ingredient due to potential health consequences from its consumption, and 2) it appears the food is fabricated from two or more ingredients and the label does not list the common or usual name of each ingredient.
LIST INGRE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
COLOR LBLG
The article appears to contain an artificial coloring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/29/2015 | 20ECT09GRAPE, TOPPING OR SYRUP | Division of Northeast Imports (DNEI) | |
| 10/29/2015 | 20LCT06ORANGE, TOPPING OR SYRUP, | Division of Northeast Imports (DNEI) | |
| 10/29/2015 | 20LCT06ORANGE, TOPPING OR SYRUP, | Division of Northeast Imports (DNEI) | |
| 4/25/2005 | 20TCT04QUINCE, TOPPING OR SYRUP | 62NEEDS FCE | New York District Office (NYK-DO) |
| 4/25/2005 | 21LCT99PIT FRUIT, TOPPING OR SYRUP, N.E.C. | 62NEEDS FCE | New York District Office (NYK-DO) |
| 4/25/2005 | 21WCT03FIG, TOPPING OR SYRUP | 62NEEDS FCE | New York District Office (NYK-DO) |
| 4/25/2005 | 21LCT99PIT FRUIT, TOPPING OR SYRUP, N.E.C. | 62NEEDS FCE | New York District Office (NYK-DO) |
Frequently Asked Questions
What is D. VOURDERIS & CO O.E.E.'s FDA import refusal history?
D. VOURDERIS & CO O.E.E. (FEI: 3004293972) has 7 FDA import refusal record(s) in our database, spanning from 4/25/2005 to 10/29/2015.
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. D. VOURDERIS & CO O.E.E.'s FEI number is 3004293972.
What types of violations has D. VOURDERIS & CO O.E.E. received?
D. VOURDERIS & CO O.E.E. has been cited for 5 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 D. VOURDERIS & CO O.E.E. come from?
All FDA import refusal data for D. VOURDERIS & CO O.E.E. 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.