Dp Inversiones, S.A.
FDA import alert and refusal historySumpango, GuatemalaFEI 3008691528
Recorded by FDA as DP INVERSIONES, S.A.
As of October 25, 2026, Dp Inversiones, S.A. (Sumpango, Guatemala) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for sugar snap peas, published by FDA on September 12, 2024, and has 14 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- Snow peas · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Dp Inversiones, S.A.
15 records, newest first. Each line links to the FDA page it came from.
2025
2024
2023
2022
2021
2020
Refusal charges, in plain English
- PESTICIDE14 refused lines
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 Dp Inversiones, S.A.
- Is Dp Inversiones, S.A. on an FDA import alert?
- Yes. As of October 25, 2026, Dp Inversiones, S.A. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for sugar snap peas; FDA published the listing on September 12, 2024.
- Has FDA refused shipments from Dp Inversiones, S.A.?
- Yes. FDA refused 14 shipment lines from Dp Inversiones, S.A. between May 29, 2020 and February 10, 2025. The most recent, on February 10, 2025, was snow peas, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Dp Inversiones, S.A.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 14 lines).
- What is Dp Inversiones, S.A.'s FEI number?
- Dp Inversiones, S.A.'s FDA Establishment Identifier (FEI) is 3008691528.
- Can shipments from Dp Inversiones, S.A. still enter the U.S.?
- Shipments of sugar snap peas from Dp Inversiones, S.A. can be detained without physical examination under Import Alert 99-05; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.