FDA Inspection 1159190 — Nipro Vascular Innovations Americas Inc

Nipro Vascular Innovations Americas Inc — FEI 3015551113

The FDA completed an inspection of Nipro Vascular Innovations Americas Inc on Dec 8, 2021 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
Dec 8, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Bedford, MA (United States)

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