FDA Import Refusal MH9-2127412-1/13/1 — GUANGDONG BIOLIGHT MEDITECH CO., LTD
The FDA refused shipment MH9-2127412-1/13/1 from GUANGDONG BIOLIGHT MEDITECH CO., LTD (China) on Aug 18, 2022. The refused product falls under Devices — MONITOR, BED PATIENT. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Aug 18, 2022
- Country
- China
- Product Category
- Devices
- Product Code
- 80KMI MONITOR, BED PATIENT
- Charges
- 118