Geodi SA
FDA import alert and refusal historyAthens, GreeceFEI 3009947529
Recorded by FDA as GEODI SA
As of October 25, 2026, Geodi SA is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 14, 2018, most often for major food allergen not declared (ALLERGEN).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vegetable protein products not elsewhere mentioned, n.e.c. · LIST INGRE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Geodi SA
2 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2018
- Import refusalRefused, Vegetable protein products not elsewhere mentioned, n.e.c.LIST INGRELACKS N/CALLERGENNUTRIT LBLNEEDS FCENO PROCESSEntry D82-2181265-3Source
Refusal charges, in plain English
- ALLERGEN1 refused line
Major food allergen not declared
The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.
- LACKS N/C1 refused line
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.
- 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).
- NEEDS FCE1 refused line
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
- NO PROCESS1 refused line
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 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 Geodi SA
- Is Geodi SA on an FDA import alert?
- No listing for Geodi SA appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Greece page.
- Has FDA refused shipments from Geodi SA?
- Yes. FDA refused 1 shipment line from Geodi SA on June 14, 2018. The most recent, on June 14, 2018, was vegetable protein products not elsewhere mentioned, n.e.c., charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Geodi SA's shipments?
- The most frequent charges are ALLERGEN (major food allergen not declared, 1 line) and LACKS N/C (net quantity statement missing, 1 line).
- When was Geodi SA last inspected by FDA?
- FDA's most recent inspection of Geodi SA with a final classification is dated February 12, 2019 and was classified NAI (No Action Indicated).
- What is Geodi SA's FEI number?
- Geodi SA's FDA Establishment Identifier (FEI) is 3009947529.
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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.