MEYOZ SUT URUNLERI VE GIDA SANAYI AS
⚠️ Moderate Risk
FEI: 3023817526 • Bursa • TURKEY
FEI Number
3023817526
Location
Bursa
Country
TURKEYAddress
Kurtulus Mah Ataturk Cas No 232 Gur, , Bursa, , 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
LACKS N/C
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(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
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.
FALSE
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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
FLAVR LBLG
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain an artificial flavoring and it fails to bear labeling stating that fact.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/10/2023 | 29AGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, NONCARBONATED | Division of West Coast Imports (DWCI) | |
| 1/10/2023 | 29AGT04SOFT DRINK, MIXED FRUIT FLAVORED, NONCARBONATED | Division of West Coast Imports (DWCI) | |
| 1/10/2023 | 29AGT01SOFT DRINK, BERRY FRUIT FLAVORED, NONCARBONATED | Division of West Coast Imports (DWCI) | |
| 1/10/2023 | 29AGT08SOFT DRINK, VINE FRUIT FLAVORED, NONCARBONATED | Division of West Coast Imports (DWCI) | |
| 1/10/2023 | 29AGT03SOFT DRINK, CORE FRUIT FLAVORED, NONCARBONATED | Division of West Coast Imports (DWCI) |
Frequently Asked Questions
What is MEYOZ SUT URUNLERI VE GIDA SANAYI AS's FDA import refusal history?
MEYOZ SUT URUNLERI VE GIDA SANAYI AS (FEI: 3023817526) has 5 FDA import refusal record(s) in our database, spanning from 1/10/2023 to 1/10/2023.
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. MEYOZ SUT URUNLERI VE GIDA SANAYI AS's FEI number is 3023817526.
What types of violations has MEYOZ SUT URUNLERI VE GIDA SANAYI AS received?
MEYOZ SUT URUNLERI VE GIDA SANAYI AS 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 MEYOZ SUT URUNLERI VE GIDA SANAYI AS come from?
All FDA import refusal data for MEYOZ SUT URUNLERI VE GIDA SANAYI AS 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.