Shrichakra Udyog Private Limited
FDA import alert and refusal historyGandhidham, IndiaFEI 3006790695
As of October 26, 2026, Shrichakra Udyog Private Limited (Gandhidham, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for sesame seed, published by FDA on June 14, 2010, 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Shrichakra Udyog Private Limited
2 records, newest first. Each line links to the FDA page it came from.
2010
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 99-19red listSesame SeedSource
Questions about Shrichakra Udyog Private Limited
- Is Shrichakra Udyog Private Limited on an FDA import alert?
- Yes. As of October 26, 2026, Shrichakra Udyog Private Limited is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for sesame seed; FDA published the listing on June 14, 2010.
- Has FDA refused shipments from Shrichakra Udyog Private Limited?
- No FDA import refusals for Shrichakra Udyog Private Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Shrichakra Udyog Private Limited last inspected by FDA?
- FDA's most recent inspection of Shrichakra Udyog Private Limited with a final classification is dated October 29, 2010 and was classified VAI (Voluntary Action Indicated).
- What is Shrichakra Udyog Private Limited's FEI number?
- Shrichakra Udyog Private Limited's FDA Establishment Identifier (FEI) is 3006790695.
- Can shipments from Shrichakra Udyog Private Limited still enter the U.S.?
- Shipments of sesame seed from Shrichakra Udyog Private Limited can be detained without physical examination under Import Alert 99-19; 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.