Surapon Foods Limited Company
FDA import alert and refusal historyMueang Samut Prakan, ThailandFEI 1000502093
Recorded by FDA as Surapon Foods Limited Company; Surapon Foods Public Company Limited
As of October 27, 2026, Surapon Foods Limited Company is on the green list of FDA Import Alert 16-18, 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 16-18 · 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 Surapon Foods Limited Company
2 records, newest first. Each line links to the FDA page it came from.
2013
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 16-18green listRaw ShrimpSource
Questions about Surapon Foods Limited Company
- Is Surapon Foods Limited Company on an FDA import alert?
- Yes. As of October 27, 2026, Surapon Foods Limited Company is on the green list of FDA Import Alert 16-18, “Raw shrimp”, for raw shrimp; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Surapon Foods Limited Company?
- No FDA import refusals for Surapon Foods Limited Company appear in FDA's refusal data since October 2016, as of October 27, 2026.
- When was Surapon Foods Limited Company last inspected by FDA?
- FDA's most recent inspection of Surapon Foods Limited Company with a final classification is dated May 10, 2013 and was classified NAI (No Action Indicated).
- What is Surapon Foods Limited Company's FEI number?
- Surapon Foods Limited Company's FDA Establishment Identifier (FEI) is 1000502093.
Buying from Surapon Foods Limited Company?
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.