FDA Inspection 629863 — OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY
The FDA completed an inspection of OLYMPUS TERUMO BIOMATERIALS CORP. MISHIMA FACTORY on October 15, 2009 in Sunto-Gun. 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
- October 15, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Sunto-Gun (Japan)