Salvatierra Group SAC
FDA import alert and refusal historyLima, PeruFEI 3013307665
Recorded by FDA as SALVATIERRA GROUP SAC
As of October 26, 2026, Salvatierra Group SAC is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on April 27, 2017, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Capsicums (cayenne chili, hot peppers), whole (spice) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Salvatierra Group SAC
3 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 3 lines in one entry: Capsicums (cayenne chili, hot peppers), whole (spice); Paprika, whole (spice)FILTHYEntry 906-0089531-5Show 3 linesHide lines
Refusal charges, in plain English
- FILTHY3 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Salvatierra Group SAC
- Is Salvatierra Group SAC on an FDA import alert?
- No listing for Salvatierra Group SAC 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 Salvatierra Group SAC?
- Yes. FDA refused 3 shipment lines from Salvatierra Group SAC on April 27, 2017. The most recent, on April 27, 2017, was capsicums (cayenne chili, hot peppers), whole (spice), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Salvatierra Group SAC's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 3 lines).
- What is Salvatierra Group SAC's FEI number?
- Salvatierra Group SAC's FDA Establishment Identifier (FEI) is 3013307665.
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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.