Paradise Exim
FDA import alert and refusal historyMandsaur, IndiaFEI 3030864896
Recorded by FDA as PARADISE EXIM
As of October 25, 2026, Paradise Exim (Mandsaur, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for quinoa, published by FDA on June 16, 2025, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- Quinoa seed (edible seed) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Paradise Exim
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 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 Paradise Exim
- Is Paradise Exim on an FDA import alert?
- Yes. As of October 25, 2026, Paradise Exim is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for quinoa; FDA published the listing on June 16, 2025.
- Has FDA refused shipments from Paradise Exim?
- Yes. FDA refused 2 shipment lines from Paradise Exim between July 7, 2025 and August 5, 2025. The most recent, on August 5, 2025, was quinoa seed (edible seed), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Paradise Exim's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Paradise Exim's FEI number?
- Paradise Exim's FDA Establishment Identifier (FEI) is 3030864896.
- Can shipments from Paradise Exim still enter the U.S.?
- Shipments of quinoa from Paradise Exim can be detained without physical examination under Import Alert 99-08; 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.