FDA Import Refusal AEK-8649304-2/1/1 — Kj Meditech
The FDA refused shipment AEK-8649304-2/1/1 from Kj Meditech (South Korea) on Jan 11, 2012. The refused product falls under Devices — SCREW, FIXATION, BONE, NON-SPINAL, METALLIC. Cited charges: 118,341 This firm has 3 other import refusals on record.
Refusal details
- Date
- Jan 11, 2012
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 87NDJ SCREW, FIXATION, BONE, NON-SPINAL, METALLIC
- Charges
- 118,341