Sandhya Marines Limited Unit 1
FDA import alert and refusal historyPalakol, IndiaFEI 3010026360
As of October 26, 2026, Sandhya Marines Limited Unit 1 is on the green list of FDA Import Alert 16-35, which exempts its listed products from detention without physical examination under that alert, 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 16-35 · green list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Sandhya Marines Limited Unit 1
3 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2013
- Import alert listingListed on Import Alert 16-35green listRaw Shrimp; Cooked ShrimpSource
Questions about Sandhya Marines Limited Unit 1
- Is Sandhya Marines Limited Unit 1 on an FDA import alert?
- Yes. As of October 26, 2026, Sandhya Marines Limited Unit 1 is on the green list of FDA Import Alert 16-35, “Raw and cooked shrimp from India”, for raw shrimp; cooked shrimp; FDA published the listing on October 9, 2013.
- Has FDA refused shipments from Sandhya Marines Limited Unit 1?
- No FDA import refusals for Sandhya Marines Limited Unit 1 appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Sandhya Marines Limited Unit 1 last inspected by FDA?
- FDA's most recent inspection of Sandhya Marines Limited Unit 1 with a final classification is dated November 22, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Sandhya Marines Limited Unit 1's FEI number?
- Sandhya Marines Limited Unit 1's FDA Establishment Identifier (FEI) is 3010026360.
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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.