Agriprocess S.A.C.
FDA import alert and refusal historyCallao, PeruFEI 3011642813
Recorded by FDA as AGRIPROCESS S.A.C.
As of October 26, 2026, Agriprocess S.A.C. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 1, 2025, most often for importer not in compliance with fsvp (FSVP VIO).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Lima bean · FSVP VIO
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Agriprocess S.A.C.
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FSVP VIO1 refused line
Importer not in compliance with FSVP
The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.
Questions about Agriprocess S.A.C.
- Is Agriprocess S.A.C. on an FDA import alert?
- No listing for Agriprocess S.A.C. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Peru page.
- Has FDA refused shipments from Agriprocess S.A.C.?
- Yes. FDA refused 1 shipment line from Agriprocess S.A.C. on July 1, 2025. The most recent, on July 1, 2025, was lima bean, charged as FSVP VIO (importer not in compliance with fsvp).
- Why did FDA refuse Agriprocess S.A.C.'s shipments?
- The most frequent charge is FSVP VIO (importer not in compliance with fsvp, 1 line).
- When was Agriprocess S.A.C. last inspected by FDA?
- FDA's most recent inspection of Agriprocess S.A.C. with a final classification is dated March 11, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Agriprocess S.A.C.'s FEI number?
- Agriprocess S.A.C.'s FDA Establishment Identifier (FEI) is 3011642813.
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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.