Va Kei Agricultural Commoities Processing Co.
FDA import alert and refusal historyZhuhai, ChinaFEI 3004332283
As of October 25, 2026, Va Kei Agricultural Commoities Processing Co. (Zhuhai, China) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for trogopterus xanthipes milne edwards (common name; "flying squirrel feces"), published by FDA on September 16, 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Va Kei Agricultural Commoities Processing Co.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listTrogopterus Xanthipes Milne Edwards (Common Name; "Flying Squirrel Feces")Source
Questions about Va Kei Agricultural Commoities Processing Co.
- Is Va Kei Agricultural Commoities Processing Co. on an FDA import alert?
- Yes. As of October 25, 2026, Va Kei Agricultural Commoities Processing Co. is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for trogopterus xanthipes milne edwards (common name; "flying squirrel feces"); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Va Kei Agricultural Commoities Processing Co.?
- No FDA import refusals for Va Kei Agricultural Commoities Processing Co. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Va Kei Agricultural Commoities Processing Co.'s FEI number?
- Va Kei Agricultural Commoities Processing Co.'s FDA Establishment Identifier (FEI) is 3004332283.
- Can shipments from Va Kei Agricultural Commoities Processing Co. still enter the U.S.?
- Shipments of trogopterus xanthipes milne edwards (common name; "flying squirrel feces") from Va Kei Agricultural Commoities Processing Co. 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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