FDA Inspection 1012036 — Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
The FDA completed an inspection of Shenzhen Mindray Bio-Medical Electronics Co., Ltd. on April 14, 2017 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
- April 14, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)