Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory
FDA import alert and refusal historyKaratagi, IndiaFEI 3010711226
As of October 27, 2026, Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory (Karatagi, India) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for sona masorii rice, published by FDA on April 1, 2014, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-08red listSona Masorii RiceSource
Questions about Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory
- Is Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory on an FDA import alert?
- Yes. As of October 27, 2026, Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for sona masorii rice; FDA published the listing on April 1, 2014.
- Has FDA refused shipments from Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory?
- No FDA import refusals for Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory's FEI number?
- Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory's FDA Establishment Identifier (FEI) is 3010711226.
- Can shipments from Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory still enter the U.S.?
- Shipments of sona masorii rice from Sri Laxmi (Lakshmi) Venkateshwar Rice Mill & Ginning Factory 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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