FDA Import Refusal M21-0744049-9/2/1 — GUANGDONG BIOLIGHT MEDITECH CO., LTD

GUANGDONG BIOLIGHT MEDITECH CO., LTD — FEI 3007305624

The FDA refused shipment M21-0744049-9/2/1 from GUANGDONG BIOLIGHT MEDITECH CO., LTD (China) on Aug 11, 2011. The refused product falls under Devices — MONITOR, BED PATIENT. Cited charges: 118,341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Aug 11, 2011
Country
China
Product Category
Devices
Product Code
80KMI MONITOR, BED PATIENT
Charges
118,341

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.