Shenzhen Rungu Food Co., Ltd
FDA import alert and refusal historyShenzhen, ChinaFEI 2000026157
As of October 26, 2026, Shenzhen Rungu Food Co., Ltd has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 9, 2021, was classified VAI (Voluntary Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Shenzhen Rungu Food Co., Ltd
3 records, newest first. Each line links to the FDA page it came from.
2021
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Shenzhen Rungu Food Co., Ltd
- Is Shenzhen Rungu Food Co., Ltd on an FDA import alert?
- No listing for Shenzhen Rungu Food Co., Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the China page.
- Has FDA refused shipments from Shenzhen Rungu Food Co., Ltd?
- No FDA import refusals for Shenzhen Rungu Food Co., Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Shenzhen Rungu Food Co., Ltd last inspected by FDA?
- FDA's most recent inspection of Shenzhen Rungu Food Co., Ltd with a final classification is dated September 9, 2021 and was classified VAI (Voluntary Action Indicated).
- What is Shenzhen Rungu Food Co., Ltd's FEI number?
- Shenzhen Rungu Food Co., Ltd's FDA Establishment Identifier (FEI) is 2000026157.
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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.