Rungroj Fish Sauce Co., Ltd.
FDA import alert and refusal historyMuaeng, ThailandFEI 3003768434
As of October 26, 2026, Rungroj Fish Sauce Co., Ltd. (Muaeng, Thailand) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for shrimp sauce mam tom bac, published by FDA on September 18, 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 45-02 · 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 Rungroj Fish Sauce Co., Ltd.
2 records, newest first. Each line links to the FDA page it came from.
2009
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 45-02red listshrimp sauce mam tom bacSource
Questions about Rungroj Fish Sauce Co., Ltd.
- Is Rungroj Fish Sauce Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Rungroj Fish Sauce Co., Ltd. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for shrimp sauce mam tom bac; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Rungroj Fish Sauce Co., Ltd.?
- No FDA import refusals for Rungroj Fish Sauce Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Rungroj Fish Sauce Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of Rungroj Fish Sauce Co., Ltd. with a final classification is dated December 4, 2009 and was classified VAI (Voluntary Action Indicated).
- What is Rungroj Fish Sauce Co., Ltd.'s FEI number?
- Rungroj Fish Sauce Co., Ltd.'s FDA Establishment Identifier (FEI) is 3003768434.
- Can shipments from Rungroj Fish Sauce Co., Ltd. still enter the U.S.?
- Shipments of shrimp sauce mam tom bac from Rungroj Fish Sauce Co., Ltd. can be detained without physical examination under Import Alert 45-02; 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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