Prawn Ceylon (Pvt.) Ltd.
FDA import alert and refusal historyMarawila, Sri LankaFEI 2000042450
Recorded by FDA as PRAWN CEYLON (PVT.) LTD.
As of October 25, 2026, Prawn Ceylon (Pvt.) Ltd. (Marawila, Sri Lanka) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for cuttlefish, published by FDA on October 29, 2009, 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 16-81 · 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 Prawn Ceylon (Pvt.) Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2015
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 16-81red listCuttlefishSource
Questions about Prawn Ceylon (Pvt.) Ltd.
- Is Prawn Ceylon (Pvt.) Ltd. on an FDA import alert?
- Yes. As of October 25, 2026, Prawn Ceylon (Pvt.) Ltd. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for cuttlefish; FDA published the listing on October 29, 2009.
- Has FDA refused shipments from Prawn Ceylon (Pvt.) Ltd.?
- No FDA import refusals for Prawn Ceylon (Pvt.) Ltd. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Prawn Ceylon (Pvt.) Ltd. last inspected by FDA?
- FDA's most recent inspection of Prawn Ceylon (Pvt.) Ltd. with a final classification is dated June 24, 2015 and was classified VAI (Voluntary Action Indicated).
- What is Prawn Ceylon (Pvt.) Ltd.'s FEI number?
- Prawn Ceylon (Pvt.) Ltd.'s FDA Establishment Identifier (FEI) is 2000042450.
- Can shipments from Prawn Ceylon (Pvt.) Ltd. still enter the U.S.?
- Shipments of cuttlefish from Prawn Ceylon (Pvt.) Ltd. can be detained without physical examination under Import Alert 16-81; 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.