FDA Inspection 761927 — Terumo Medical Products (Hangzhou) Co., Ltd.
The FDA completed an inspection of Terumo Medical Products (Hangzhou) Co., Ltd. on December 16, 2011 in Hangzhou. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- December 16, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Hangzhou (China)