Interfood Shareholding
FDA import alert and refusal historyBien Hoa, VietnamFEI 3013300482
As of October 26, 2026, Interfood Shareholding (Bien Hoa, Vietnam) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for coconut water w/pulp (meat), published by FDA on October 2, 2015, 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 99-39 · 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 Interfood Shareholding
2 records, newest first. Each line links to the FDA page it came from.
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2015
- Import alert listingListed on Import Alert 99-39red listCoconut water w/pulp (meat)Source
Questions about Interfood Shareholding
- Is Interfood Shareholding on an FDA import alert?
- Yes. As of October 26, 2026, Interfood Shareholding is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for coconut water w/pulp (meat); FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Interfood Shareholding?
- No FDA import refusals for Interfood Shareholding appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Interfood Shareholding last inspected by FDA?
- FDA's most recent inspection of Interfood Shareholding with a final classification is dated September 20, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Interfood Shareholding's FEI number?
- Interfood Shareholding's FDA Establishment Identifier (FEI) is 3013300482.
- Can shipments from Interfood Shareholding still enter the U.S.?
- Shipments of coconut water w/pulp (meat) from Interfood Shareholding can be detained without physical examination under Import Alert 99-39; 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.