Alimentos SAS S.A.S
FDA import alert and refusal historyBogota, ColombiaFEI 3011283383
As of October 26, 2026, Alimentos SAS S.A.S is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 16, 2021, 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
- Strawberries (berry purees) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Alimentos SAS S.A.S
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE1 refused line
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 Alimentos SAS S.A.S
- Is Alimentos SAS S.A.S on an FDA import alert?
- No listing for Alimentos SAS S.A.S appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
- Has FDA refused shipments from Alimentos SAS S.A.S?
- Yes. FDA refused 1 shipment line from Alimentos SAS S.A.S on December 16, 2021. The most recent, on December 16, 2021, was strawberries (berry purees), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Alimentos SAS S.A.S's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- When was Alimentos SAS S.A.S last inspected by FDA?
- FDA's most recent inspection of Alimentos SAS S.A.S with a final classification is dated April 19, 2018 and was classified VAI (Voluntary Action Indicated).
- What is Alimentos SAS S.A.S's FEI number?
- Alimentos SAS S.A.S's FDA Establishment Identifier (FEI) is 3011283383.
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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.