FDA Warning Letter — AZ Instrument (Shen Zhen) Co., Ltd.

Case 162012 — FEI 3005257705

The FDA took a Warning Letter action against AZ Instrument (Shen Zhen) Co., Ltd. on March 4, 2011 (Shenzhen, China). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
AZ Instrument (Shen Zhen) Co., Ltd.
Date
March 4, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Shenzhen (China)