FDA Inspection 630365 — Nipro Vascular Innovations Americas Inc
The FDA completed an inspection of Nipro Vascular Innovations Americas Inc on Oct 29, 2009 in Bedford, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Oct 29, 2009
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Bedford, MA (United States)