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Narin BYS

⚠️ Moderate Risk

FEI: 3008214147 • Akdeniz, Mersin • TURKEY

FEI

FEI Number

3008214147

📍

Location

Akdeniz, Mersin

🇹🇷

Country

TURKEY
🏢

Address

Plaza No:66 K:20 D 39/40, , Akdeniz, Mersin, Turkey

Moderate Risk

FDA Import Risk Assessment

45.4
LowModerateHighCritical

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

Statistics

15
Total Refusals
9
Unique Violations
8/21/2015
Latest Refusal
3/5/2007
Earliest Refusal

Score Breakdown

Violation Severity
75.7×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
17.7×10%
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

97×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

116×

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).

3212×

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.

33202×

TRANSFAT

The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].

4822×

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.

4881×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

621×

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).

831×

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.

2181×

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.

Refusal History

DateProductViolationsDivision
8/21/2015
23MCT01SESAME SEED PASTE (E.G., TAHINA), EDIBLE SEED PROD.
9SALMONELLA
Division of Northeast Imports (DNEI)
4/9/2015
23RGT02SESAME SEED (EDIBLE SEED PASTE)
9SALMONELLA
New York District Office (NYK-DO)
3/31/2015
23MGT01SESAME SEED PASTE (E.G., TAHINA), EDIBLE SEED PROD.
9SALMONELLA
Chicago District Office (CHI-DO)
2/13/2015
23MHT01SESAME SEED PASTE (E.G., TAHINA), EDIBLE SEED PROD.
9SALMONELLA
Division of Northeast Imports (DNEI)
2/13/2015
23MHT01SESAME SEED PASTE (E.G., TAHINA), EDIBLE SEED PROD.
9SALMONELLA
New York District Office (NYK-DO)
4/17/2013
23MGH01SESAME SEED PASTE (E.G., TAHINA), EDIBLE SEED PROD.
9SALMONELLA
New York District Office (NYK-DO)
6/28/2012
23RHT02SESAME SEED (EDIBLE SEED PASTE)
9SALMONELLA
Baltimore District Office (BLT-DO)
4/19/2011
24CGT06CHICK PEA, WITH SAUCE
11UNSAFE COL
New York District Office (NYK-DO)
4/19/2011
24CGT06CHICK PEA, WITH SAUCE
11UNSAFE COL
New York District Office (NYK-DO)
4/19/2011
24CGT06CHICK PEA, WITH SAUCE
11UNSAFE COL
New York District Office (NYK-DO)
4/19/2011
24CGT07KIDNEY BEAN, WITH SAUCE
11UNSAFE COL
New York District Office (NYK-DO)
7/24/2007
21GGE09OLIVES (PIT FRUIT)
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
4/26/2007
23BGT12WALNUTS, BLACK, ENGLISH OR PERSIAN, SHELLED
218LIST INGRE
321LACKS N/C
3320TRANSFAT
482NUTRIT LBL
488HEALTH C
Los Angeles District Office (LOS-DO)
3/30/2007
20KGT04LEMON, CITRUS FRUIT JUICES OR CONCENTRATES
11UNSAFE COL
Los Angeles District Office (LOS-DO)
3/5/2007
23BGT12WALNUTS, BLACK, ENGLISH OR PERSIAN, SHELLED
11UNSAFE COL
321LACKS N/C
3320TRANSFAT
482NUTRIT LBL
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Narin BYS's FDA import refusal history?

Narin BYS (FEI: 3008214147) has 15 FDA import refusal record(s) in our database, spanning from 3/5/2007 to 8/21/2015.

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. Narin BYS's FEI number is 3008214147.

What types of violations has Narin BYS received?

Narin BYS has been cited for 9 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 Narin BYS come from?

All FDA import refusal data for Narin BYS 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.