FDA Inspection 1227468 — Nipro Vascular Innovations Americas Inc

Nipro Vascular Innovations Americas Inc — FEI 3015551113

The FDA completed an inspection of Nipro Vascular Innovations Americas Inc on Jan 9, 2024 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
Jan 9, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Bedford, MA (United States)

Additional details

Sponsor, Contract Research Organization

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.