Cuscatlan Manufacturing SA de CV
FDA import alert and refusal historySan Salvador, El SalvadorFEI 3015525311
Recorded by FDA as CUSCATLAN MANUFACTURING SA DE CV
As of October 26, 2026, Cuscatlan Manufacturing SA de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 31, 2021, 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
- Tamarind, jam, jelly, preserves, marmalade, butter or candied · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Cuscatlan Manufacturing SA de CV
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
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 Cuscatlan Manufacturing SA de CV
- Is Cuscatlan Manufacturing SA de CV on an FDA import alert?
- No listing for Cuscatlan Manufacturing SA de CV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the El Salvador page.
- Has FDA refused shipments from Cuscatlan Manufacturing SA de CV?
- Yes. FDA refused 1 shipment line from Cuscatlan Manufacturing SA de CV on August 31, 2021. The most recent, on August 31, 2021, was tamarind, jam, jelly, preserves, marmalade, butter or candied, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Cuscatlan Manufacturing SA de CV's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- What is Cuscatlan Manufacturing SA de CV's FEI number?
- Cuscatlan Manufacturing SA de CV's FDA Establishment Identifier (FEI) is 3015525311.
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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.