FDA Inspection 629476 — NIPRO CORP.
The FDA completed an inspection of NIPRO CORP. on October 29, 2009 in Odate. 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 29, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Odate (Japan)