FDA Inspection 1069150 — Suzhou Kangli Orthopaedics Instrument Co., Ltd.
The FDA completed an inspection of Suzhou Kangli Orthopaedics Instrument Co., Ltd. on Jun 14, 2018 in Suzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 14, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Suzhou (China)