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REAL TASTE GIDA EMLAK TURIZM ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI

⚠️ Moderate Risk

FEI: 3027605095 • Esenyurt, Istanbul • TURKEY

FEI

FEI Number

3027605095

📍

Location

Esenyurt, Istanbul

🇹🇷

Country

TURKEY
🏢

Address

No:9-1 Zafer Mahallesi, 146. Sokak C Blok, Esenyurt, Istanbul, Turkey

Moderate Risk

FDA Import Risk Assessment

49.1
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

3
Total Refusals
4
Unique Violations
10/2/2023
Latest Refusal
10/2/2023
Earliest Refusal

Score Breakdown

Violation Severity
71.3×40%
Refusal Volume
22.3×30%
Recency
54.5×20%
Frequency
30.0×10%
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

4823×

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.

2412×

PESTICIDE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:

2452×

EXCESS SUL

The article appears to contain excessive sulfites, a poisonous and deleterious substance which may render it injurious to health.

20401×

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.

Refusal History

DateProductViolationsDivision
10/2/2023
21HGT01APRICOT, DRIED OR PASTE
2040SULFITELBL
245EXCESS SUL
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/2/2023
23RCT02SESAME SEED (EDIBLE SEED PASTE)
241PESTICIDE
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/2/2023
20AGT10RAISINS (DRIED GRAPES) (BERRY)
241PESTICIDE
245EXCESS SUL
482NUTRIT LBL
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is REAL TASTE GIDA EMLAK TURIZM ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI's FDA import refusal history?

REAL TASTE GIDA EMLAK TURIZM ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI (FEI: 3027605095) has 3 FDA import refusal record(s) in our database, spanning from 10/2/2023 to 10/2/2023.

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. REAL TASTE GIDA EMLAK TURIZM ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI's FEI number is 3027605095.

What types of violations has REAL TASTE GIDA EMLAK TURIZM ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI received?

REAL TASTE GIDA EMLAK TURIZM ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI has been cited for 4 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 REAL TASTE GIDA EMLAK TURIZM ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI come from?

All FDA import refusal data for REAL TASTE GIDA EMLAK TURIZM ITHALAT IHRACAT SANAYI VE TICARET LIMITED SIRKETI 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.