FDA Warning Letter — GUANGDONG BIOLIGHT MEDITECH CO., LTD

Case 381918 — FEI 3007305624

The FDA took a Warning Letter action against GUANGDONG BIOLIGHT MEDITECH CO., LTD on Jan 2, 2013 (Zhuhai, China). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action details

Facility
GUANGDONG BIOLIGHT MEDITECH CO., LTD
Date
Jan 2, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Zhuhai (China)

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