casa evelyn
FDA import alert and refusal historySanto Domingo, Dominican RepublicFEI 3018106077
As of October 26, 2026, casa evelyn is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on January 8, 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
- Chocolate candy pieces, without nuts and fruit · FSVP VIO
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for casa evelyn
3 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 3 lines in one entry: Chocolate candy pieces, without nuts and fruit; Mixed spices and seasoning with salt, n.e.c. and 1 moreFSVP VIOEntry J60-0044826-2Show 3 linesHide lines
Refusal charges, in plain English
- FSVP VIO3 refused lines
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 casa evelyn
- Is casa evelyn on an FDA import alert?
- No listing for casa evelyn appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Dominican Republic page.
- Has FDA refused shipments from casa evelyn?
- Yes. FDA refused 3 shipment lines from casa evelyn on January 8, 2025. The most recent, on January 8, 2025, was chocolate candy pieces, without nuts and fruit, charged as FSVP VIO (importer not in compliance with fsvp).
- Why did FDA refuse casa evelyn's shipments?
- The most frequent charge is FSVP VIO (importer not in compliance with fsvp, 3 lines).
- What is casa evelyn's FEI number?
- casa evelyn's FDA Establishment Identifier (FEI) is 3018106077.
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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.