Vinh Hiep Co Ltd
FDA import alert and refusal historyPleiku City, VietnamFEI 3008326047
As of October 26, 2026, Vinh Hiep Co Ltd (Pleiku City, Vietnam) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for black pepper, published by FDA on May 26, 2016, 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 99-19 · 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 Vinh Hiep Co Ltd
3 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2018
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2016
- Import alert listingListed on Import Alert 99-19red listBlack pepperSource
Questions about Vinh Hiep Co Ltd
- Is Vinh Hiep Co Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Vinh Hiep Co Ltd is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for black pepper; FDA published the listing on May 26, 2016.
- Has FDA refused shipments from Vinh Hiep Co Ltd?
- No FDA import refusals for Vinh Hiep Co Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Vinh Hiep Co Ltd last inspected by FDA?
- FDA's most recent inspection of Vinh Hiep Co Ltd with a final classification is dated April 16, 2019 and was classified NAI (No Action Indicated).
- What is Vinh Hiep Co Ltd's FEI number?
- Vinh Hiep Co Ltd's FDA Establishment Identifier (FEI) is 3008326047.
- Can shipments from Vinh Hiep Co Ltd still enter the U.S.?
- Shipments of black pepper from Vinh Hiep Co Ltd can be detained without physical examination under Import Alert 99-19; 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.