Kenko Corporation
FDA import alert and refusal historyChiyoda, JapanFEI 3004263613
As of October 26, 2026, Kenko Corporation is on the green list of FDA Import Alert 16-02, which exempts its listed products from detention without physical examination under that alert, 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 16-02 · green list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Kenko Corporation
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-02green listShark Cartilage PowderSource
Questions about Kenko Corporation
- Is Kenko Corporation on an FDA import alert?
- Yes. As of October 26, 2026, Kenko Corporation is on the green list of FDA Import Alert 16-02, “Dried shark fins, fish maws and shark cartilage: filth”, for shark cartilage powder; FDA published the listing on September 10, 2009.
- Has FDA refused shipments from Kenko Corporation?
- No FDA import refusals for Kenko Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Kenko Corporation's FEI number?
- Kenko Corporation's FDA Establishment Identifier (FEI) is 3004263613.
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