Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi
FDA import alert and refusal historyMenemen, TurkeyFEI 3007849293
As of October 26, 2026, Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi (Menemen, Turkey) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for lemon juice, published by FDA on March 30, 2013, and has 4 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- Pepper sauce (hot, mild, etc.) · LACKS N/C
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi
6 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 3 lines in one entry: Pepper sauce (hot, mild, etc.)LACKS N/CNUTRIT LBLNO PROCESSEntry 9DH-0071163-5Show 3 linesHide lines
- Refused, Pepper sauce (hot, mild, etc.)LACKS N/CNUTRIT LBLNO PROCESSEntry 9DH-0071163-5Source
- Refused, Pepper sauce (hot, mild, etc.)LACKS N/CNUTRIT LBLNO PROCESSEntry 9DH-0071163-5Source
- Refused, Pepper sauce (hot, mild, etc.)LACKS N/CNUTRIT LBLNO PROCESSEntry 9DH-0071163-5Source
2023
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2021
- Import refusalRefused, Salt (table salt) n.e.c.UNSAFE COLEntry DP4-8424342-4Source
2013
- Import alert listingListed on Import Alert 45-02red listLemon JuiceSource
Refusal charges, in plain English
- LACKS N/C3 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- NO PROCESS3 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
- NUTRIT LBL3 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi
- Is Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi on an FDA import alert?
- Yes. As of October 26, 2026, Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for lemon juice; FDA published the listing on March 30, 2013.
- Has FDA refused shipments from Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi?
- Yes. FDA refused 4 shipment lines from Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi between October 19, 2021 and July 24, 2025. The most recent, on July 24, 2025, was pepper sauce (hot, mild, etc.), charged as LACKS N/C (net quantity statement missing).
- Why did FDA refuse Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi's shipments?
- The most frequent charges are LACKS N/C (net quantity statement missing, 3 lines) and NO PROCESS (no scheduled process filed, 3 lines).
- When was Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi last inspected by FDA?
- FDA's most recent inspection of Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi with a final classification is dated July 13, 2023 and was classified NAI (No Action Indicated).
- What is Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi's FEI number?
- Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi's FDA Establishment Identifier (FEI) is 3007849293.
- Can shipments from Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi still enter the U.S.?
- Shipments of lemon juice from Kozmopolitan Gida Sanayi Ve Ticaret Anonim Sirketi can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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