Relish Agro Food
FDA import alert and refusal historyAmreli, IndiaFEI 3007323225
As of October 26, 2026, Relish Agro Food (Amreli, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for palak chopped spinach, published by FDA on April 26, 2013, and has 1 FDA import refusal 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
- Tamarind, jam, jelly, preserves, marmalade, butter or candied · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Relish Agro Food
2 records, newest first. Each line links to the FDA page it came from.
2021
2013
- Import alert listingListed on Import Alert 99-08red listPalak Chopped SpinachSource
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 Relish Agro Food
- Is Relish Agro Food on an FDA import alert?
- Yes. As of October 26, 2026, Relish Agro Food is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for palak chopped spinach; FDA published the listing on April 26, 2013.
- Has FDA refused shipments from Relish Agro Food?
- Yes. FDA refused 1 shipment line from Relish Agro Food on November 5, 2021. The most recent, on November 5, 2021, was tamarind, jam, jelly, preserves, marmalade, butter or candied, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Relish Agro Food's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- What is Relish Agro Food's FEI number?
- Relish Agro Food's FDA Establishment Identifier (FEI) is 3007323225.
- Can shipments from Relish Agro Food still enter the U.S.?
- Shipments of palak chopped spinach from Relish Agro Food 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.