FDA Inspection 1013359 — Nipro Vascular Innovations Americas Inc
The FDA completed an inspection of Nipro Vascular Innovations Americas Inc on Jun 2, 2017 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
- Jun 2, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Bedford, MA (United States)