FDA Import Refusal AEK-1209351-1/1/1 — GUANGDONG BIOLIGHT MEDITECH CO., LTD

GUANGDONG BIOLIGHT MEDITECH CO., LTD — FEI 3007305624

The FDA refused shipment AEK-1209351-1/1/1 from GUANGDONG BIOLIGHT MEDITECH CO., LTD (China) on Jun 26, 2015. The refused product falls under Devices — OXIMETER. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jun 26, 2015
Country
China
Product Category
Devices
Product Code
74DQA OXIMETER
Charges
341

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