Orizon S.A.
FDA import alert and refusal historyCoronel, ChileFEI 3004272256
Recorded by FDA as ORIZON S.A.
As of October 26, 2026, Orizon S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on July 14, 2023, was classified VAI (Voluntary Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Orizon S.A.
3 records, newest first. Each line links to the FDA page it came from.
2023
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2011
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Questions about Orizon S.A.
- Is Orizon S.A. on an FDA import alert?
- No listing for Orizon 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 Chile page.
- Has FDA refused shipments from Orizon S.A.?
- No FDA import refusals for Orizon S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Orizon S.A. last inspected by FDA?
- FDA's most recent inspection of Orizon S.A. with a final classification is dated July 14, 2023 and was classified VAI (Voluntary Action Indicated).
- What is Orizon S.A.'s FEI number?
- Orizon S.A.'s FDA Establishment Identifier (FEI) is 3004272256.
Buying from Orizon S.A.?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.