FDA Import Refusal AEK-9193370-1/1/1 — LaserOptek
The FDA refused shipment AEK-9193370-1/1/1 from LaserOptek (South Korea) on Aug 26, 2013. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charges: 341,476,508 This firm has 1 other import refusal on record.
Refusal details
- Date
- Aug 26, 2013
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 79GEX POWERED LASER SURGICAL INSTRUMENTS
- Charges
- 341,476,508