FDA Inspection 629476 — NIPRO CORP.
The FDA completed an inspection of NIPRO CORP. on Oct 29, 2009 in Odate. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection details
- Classification
- Official Action Indicated (OAI)
- End Date
- Oct 29, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Odate (Japan)