Agricola y Ganadera Chavin de Huantar SA
FDA import alert and refusal historyLima, PeruFEI 3019521222
Recorded by FDA as AGRICOLA Y GANADERA CHAVIN DE HUANTAR SA
As of October 27, 2026, Agricola y Ganadera Chavin de Huantar SA is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 28, 2022, 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) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Agricola y Ganadera Chavin de Huantar SA
1 record, 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 Agricola y Ganadera Chavin de Huantar SA
- Is Agricola y Ganadera Chavin de Huantar SA on an FDA import alert?
- No listing for Agricola y Ganadera Chavin de Huantar SA appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Peru page.
- Has FDA refused shipments from Agricola y Ganadera Chavin de Huantar SA?
- Yes. FDA refused 1 shipment line from Agricola y Ganadera Chavin de Huantar SA on March 28, 2022. The most recent, on March 28, 2022, was strawberries (berry), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Agricola y Ganadera Chavin de Huantar SA's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is Agricola y Ganadera Chavin de Huantar SA's FEI number?
- Agricola y Ganadera Chavin de Huantar SA's FDA Establishment Identifier (FEI) is 3019521222.
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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.