Intimex Hochiminh
FDA import alert and refusal historyHochiminh City, VietnamFEI 3004270695
As of October 26, 2026, Intimex Hochiminh (Hochiminh City, Vietnam) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for dried tapioca pearl; shrimp paste (preserved shrimp), 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 NAI (No Action Indicated)
Every FDA record for Intimex Hochiminh
2 records, newest first. Each line links to the FDA page it came from.
2011
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 45-02red listdried tapioca pearl; shrimp paste (preserved shrimp)Source
Questions about Intimex Hochiminh
- Is Intimex Hochiminh on an FDA import alert?
- Yes. As of October 26, 2026, Intimex Hochiminh is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for dried tapioca pearl; shrimp paste (preserved shrimp); FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Intimex Hochiminh?
- No FDA import refusals for Intimex Hochiminh appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Intimex Hochiminh last inspected by FDA?
- FDA's most recent inspection of Intimex Hochiminh with a final classification is dated September 16, 2011 and was classified NAI (No Action Indicated).
- What is Intimex Hochiminh's FEI number?
- Intimex Hochiminh's FDA Establishment Identifier (FEI) is 3004270695.
- Can shipments from Intimex Hochiminh still enter the U.S.?
- Shipments of dried tapioca pearl; shrimp paste (preserved shrimp) from Intimex Hochiminh 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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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.