FDA Import Refusal AEK-8498429-1/12/1 — BODITECHMED INC
The FDA refused shipment AEK-8498429-1/12/1 from BODITECHMED INC (South Korea) on May 16, 2025. The refused product falls under Devices — IN VITRO TEST KITS, INDIVIDUAL (NONHUMAN). Cited charge: 118
Refusal Details
- Date
- May 16, 2025
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 68SYG01 IN VITRO TEST KITS, INDIVIDUAL (NONHUMAN)
- Charges
- 118