FDA inspection

Stryker Spine: FDA inspection ending Mar 11, 2016

FDA inspection 965950 · No Action Indicated (NAI) · Allendale, NJ

Key facts

Inspection ID 965950
Firm Stryker Spine
FEI number 3004024955
Address 2 Pearl Ct
City Allendale
State NJ
ZIP 07401
Country United States
Fiscal year 2016
Inspection end date Mar 11, 2016
Classification No Action Indicated (NAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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