FDA inspection

Nipro Vascular Innovations Americas Inc: FDA inspection ending Jun 2, 2017

FDA inspection 1013359 · No Action Indicated (NAI) · Bedford, MA

Key facts

Inspection ID 1013359
Firm Nipro Vascular Innovations Americas Inc
FEI number 3015551113
Address 28 Crosby Dr Ste 100
City Bedford
State MA
ZIP 01730
Country United States
Fiscal year 2017
Inspection end date Jun 2, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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