Pari India
FDA import alert and refusal historyAmritsar, IndiaFEI 3012346884
Recorded by FDA as PARI INDIA
As of October 26, 2026, Pari India (AMRITSAR, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for basmati rice, published by FDA on July 3, 2018, 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
- Rice, basmati, processed (packaged) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Pari India
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 Pari India
- Is Pari India on an FDA import alert?
- Yes. As of October 26, 2026, Pari India is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for basmati rice; FDA published the listing on July 3, 2018.
- Has FDA refused shipments from Pari India?
- Yes. FDA refused 2 shipment lines from Pari India between July 10, 2018 and November 13, 2018. The most recent, on November 13, 2018, was rice, basmati, processed (packaged), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Pari India's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Pari India's FEI number?
- Pari India's FDA Establishment Identifier (FEI) is 3012346884.
- Can shipments from Pari India still enter the U.S.?
- Shipments of basmati rice from Pari India 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.