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Alterra S.A.

FDA import alert and refusal historyGiannitsa, GreeceFEI 3005204525

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Example subjectAlterra S.A added to Import Alert 16-129 (red list)

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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

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source
  2. Import refusal
    Refused, Spinach (leaf & stem vegetable)UNSAFE ADDEntry 85R-0957532-7
    Source

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.