FDA Inspection 911601 — Guangzhou T.K Medical Instrument Co., Ltd.
The FDA completed an inspection of Guangzhou T.K Medical Instrument Co., Ltd. on January 15, 2015 in Guangzhou. 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
- January 15, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Guangzhou (China)