FDA Inspection 891964 — AZ Instrument (Shen Zhen) Co., Ltd.
The FDA completed an inspection of AZ Instrument (Shen Zhen) Co., Ltd. on July 16, 2014 in Shenzhen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 16, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Shenzhen (China)