Alterra S.A.
FDA import alert and refusal historyGiannitsa, GreeceFEI 3005204525
As of October 26, 2026, Alterra S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 2, 2019, most often for food additive unsafe under section 409 (UNSAFE ADD).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Spinach (leaf & stem vegetable) · UNSAFE ADD
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Alterra S.A.
2 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
- Import refusalRefused, Spinach (leaf & stem vegetable)UNSAFE ADDEntry 85R-0957532-7Source
Refusal charges, in plain English
- UNSAFE ADD1 refused line
Food additive unsafe under section 409
The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.
Questions about Alterra S.A.
- Is Alterra S.A. on an FDA import alert?
- No listing for Alterra S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Greece page.
- Has FDA refused shipments from Alterra S.A.?
- Yes. FDA refused 1 shipment line from Alterra S.A. on August 2, 2019. The most recent, on August 2, 2019, was spinach (leaf & stem vegetable), charged as UNSAFE ADD (food additive unsafe under section 409).
- Why did FDA refuse Alterra S.A.'s shipments?
- The most frequent charge is UNSAFE ADD (food additive unsafe under section 409, 1 line).
- When was Alterra S.A. last inspected by FDA?
- FDA's most recent inspection of Alterra S.A. with a final classification is dated August 6, 2019 and was classified NAI (No Action Indicated).
- What is Alterra S.A.'s FEI number?
- Alterra S.A.'s FDA Establishment Identifier (FEI) is 3005204525.
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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.