FDA Import Refusal AEK-0251317-1/1/1 — Chungwoo Co Ltd
The FDA refused shipment AEK-0251317-1/1/1 from Chungwoo Co Ltd (South Korea) on Jan 16, 2015. The refused product falls under Devices — STIMULATOR, INTRAMUSCULAR, AUTOMATIC. Cited charges: 118,3280,341,508 This firm has 1 other import refusal on record.
Refusal details
- Date
- Jan 16, 2015
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 80NRW STIMULATOR, INTRAMUSCULAR, AUTOMATIC
- Charges
- 118,3280,341,508