Georgoudis S.A.
FDA import alert and refusal historyVelestino, GreeceFEI 2000008463
Recorded by FDA as GEORGOUDIS S.A.
As of October 25, 2026, Georgoudis S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between May 30, 2017 and July 13, 2017, most often for pesticide chemical residue (PESTICIDE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Olives, dried or paste · PESTICIDE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Georgoudis S.A.
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Georgoudis S.A.
- Is Georgoudis S.A. on an FDA import alert?
- No listing for Georgoudis S.A. 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 Georgoudis S.A.?
- Yes. FDA refused 2 shipment lines from Georgoudis S.A. between May 30, 2017 and July 13, 2017. The most recent, on July 13, 2017, was olives, dried or paste, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Georgoudis S.A.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- When was Georgoudis S.A. last inspected by FDA?
- FDA's most recent inspection of Georgoudis S.A. with a final classification is dated June 8, 2016 and was classified NAI (No Action Indicated).
- What is Georgoudis S.A.'s FEI number?
- Georgoudis S.A.'s FDA Establishment Identifier (FEI) is 2000008463.
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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.