M/S.Devi Fisheries Limited
FDA import alert and refusal historyViskakhapatnam, IndiaFEI 3004045117
Recorded by FDA as M/S.DEVI FISHERIES LIMITED
As of October 26, 2026, M/S.Devi Fisheries 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 VAI (Voluntary Action Indicated)
Every FDA record for M/S.Devi Fisheries Limited
2 records, newest first. Each line links to the FDA page it came from.
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 ShrimpSource
Questions about M/S.Devi Fisheries Limited
- Is M/S.Devi Fisheries Limited on an FDA import alert?
- Yes. As of October 26, 2026, M/S.Devi Fisheries Limited is on the green list of FDA Import Alert 16-35, “Raw and cooked shrimp from India”, for raw shrimp; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from M/S.Devi Fisheries Limited?
- No FDA import refusals for M/S.Devi Fisheries Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was M/S.Devi Fisheries Limited last inspected by FDA?
- FDA's most recent inspection of M/S.Devi Fisheries Limited with a final classification is dated December 1, 2014 and was classified VAI (Voluntary Action Indicated).
- What is M/S.Devi Fisheries Limited's FEI number?
- M/S.Devi Fisheries Limited's FDA Establishment Identifier (FEI) is 3004045117.
Buying from M/S.Devi Fisheries Limited?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.