Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1
FDA import alert and refusal historyAkhisar, TurkeyFEI 3015290259
As of October 27, 2026, Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 29, 2024, most often for manufacturer name and address missing (LACKS FIRM).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Gel cups, fruit flavored · LIST INGRE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1
2 records, newest first. Each line links to the FDA page it came from.
2025
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2024
- Import refusalRefused, Gel cups, fruit flavoredLIST INGRELACKS FIRMNUTRIT LBLEntry D99-6631401-4Source
Refusal charges, in plain English
- LACKS FIRM1 refused line
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
Questions about Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1
- Is Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 on an FDA import alert?
- No listing for Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Turkey page.
- Has FDA refused shipments from Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1?
- Yes. FDA refused 1 shipment line from Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 on October 29, 2024. The most recent, on October 29, 2024, was gel cups, fruit flavored, charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1's shipments?
- The most frequent charges are LACKS FIRM (manufacturer name and address missing, 1 line) and LIST INGRE (ingredients not listed, 1 line).
- When was Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 last inspected by FDA?
- FDA's most recent inspection of Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1 with a final classification is dated May 14, 2025 and was classified NAI (No Action Indicated).
- What is Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1's FEI number?
- Kervan Gida Sanayi ve Ticaret A.S. Akhisar Factory 1's FDA Establishment Identifier (FEI) is 3015290259.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.