FDA inspection

Stereotaxis Inc: FDA inspection ending Aug 31, 2004

FDA inspection 343671 · No Action Indicated (NAI) · Saint Louis, MO

Key facts

Inspection ID 343671
Firm Stereotaxis Inc
FEI number 3003084417
Address 710 N Tucker Blvd Ste 110
City Saint Louis
State MO
ZIP 63101-1150
Fiscal year 2004
Inspection end date Aug 31, 2004
Classification No Action Indicated (NAI)
Project area Product Evaluation: Med Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes 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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