FDA Import Refusal AEK-5634157-8/11/1 — Bistos Co Ltd
The FDA refused shipment AEK-5634157-8/11/1 from Bistos Co Ltd (South Korea) on Feb 26, 2019. The refused product falls under Devices — SYSTEM, MONITORING, PERINATAL. Cited charge: 341 This firm has 3 other import refusals on record.
Refusal details
- Date
- Feb 26, 2019
- Country
- South Korea
- Product Category
- Devices
- Product Code
- 85HGM SYSTEM, MONITORING, PERINATAL
- Charges
- 341