FDA Inspection 1026794 — Sunny Medical Device (Shenzhen) Co., Ltd.
The FDA completed an inspection of Sunny Medical Device (Shenzhen) Co., Ltd. on August 17, 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
- August 17, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Shenzhen (China)