Del Tropico S.A.
FDA import alert and refusal historyGutatemala, GuatemalaFEI 3010664055
As of October 26, 2026, Del Tropico S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between May 10, 2018 and February 6, 2019, 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
- Cardamon, whole (spice) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Del Tropico S.A.
3 records, newest first. Each line links to the FDA page it came from.
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.
- LACKS N/C1 refused line
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
Questions about Del Tropico S.A.
- Is Del Tropico S.A. on an FDA import alert?
- No listing for Del Tropico S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
- Has FDA refused shipments from Del Tropico S.A.?
- Yes. FDA refused 3 shipment lines from Del Tropico S.A. between May 10, 2018 and February 6, 2019. The most recent, on February 6, 2019, was cardamon, whole (spice), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Del Tropico S.A.'s shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 3 lines) and LACKS N/C (net quantity statement missing, 1 line).
- What is Del Tropico S.A.'s FEI number?
- Del Tropico S.A.'s FDA Establishment Identifier (FEI) is 3010664055.
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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.