FDA Import Refusal AEK-3277121-2/12/1D — Mika Medical Co Ltd
The FDA refused shipment AEK-3277121-2/12/1D from Mika Medical Co Ltd (South Korea) on May 18, 2023. The refused product falls under Devices — NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE. Cited charge: 237 This firm has 1 other import refusal on record.
Refusal details
- Date
- May 18, 2023
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 79GAA NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE
- Charges
- 237