The Waterbase Limited
FDA import alert and refusal historyNellore, IndiaFEI 3000138421
As of October 26, 2026, The Waterbase Limited 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 NAI (No Action Indicated)
Every FDA record for The Waterbase Limited
3 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2014
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 16-35green listRaw Shrimp; Shrimp & Prawns; Heat Treated; Shrimp and prawns; Aquaculture Harvested Fishery/Seafood Products; Heat TreatedSource
Questions about The Waterbase Limited
- Is The Waterbase Limited on an FDA import alert?
- Yes. As of October 26, 2026, The Waterbase Limited is on the green list of FDA Import Alert 16-35, “Raw and cooked shrimp from India”, for raw shrimp; shrimp & prawns; heat treated; shrimp and prawns; aquaculture harvested fishery/seafood products; heat treated; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from The Waterbase Limited?
- No FDA import refusals for The Waterbase Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was The Waterbase Limited last inspected by FDA?
- FDA's most recent inspection of The Waterbase Limited with a final classification is dated September 17, 2019 and was classified NAI (No Action Indicated).
- What is The Waterbase Limited's FEI number?
- The Waterbase Limited's FDA Establishment Identifier (FEI) is 3000138421.
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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.