FDA inspection

Stryker Neurovascular, Inc.: FDA inspection ending Dec 2, 2015

FDA inspection 956410 · No Action Indicated (NAI) · Salt Lake City, UT

Key facts

Inspection ID 956410
Firm Stryker Neurovascular, Inc.
FEI number 3012931345
Address 2405 W Orton Cir
City Salt Lake City
State UT
ZIP 84120
Country United States
Fiscal year 2016
Inspection end date Dec 2, 2015
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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