FDA Inspection 948623 — Terumo Medical Products (Hangzhou) Co., Ltd.
The FDA completed an inspection of Terumo Medical Products (Hangzhou) Co., Ltd. on October 29, 2015 in Hangzhou. 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
- October 29, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hangzhou (China)