FDA inspection

Stryker Spine: FDA inspection ending Aug 1, 2019

FDA inspection 1099091 · No Action Indicated (NAI) · Allendale, NJ

Key facts

Inspection ID 1099091
Firm Stryker Spine
FEI number 3004024955
Address 2 Pearl Ct
City Allendale
State NJ
ZIP 07401
Country United States
Fiscal year 2019
Inspection end date Aug 1, 2019
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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