FDA Inspection 1062256 — Terumo Medical Products (Hangzhou) Co., Ltd.
The FDA completed an inspection of Terumo Medical Products (Hangzhou) Co., Ltd. on July 25, 2018 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
- July 25, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hangzhou (China)