FDA inspection

BIOTRONIK Inc: FDA inspection ending Mar 7, 2014

FDA inspection 869588 · No Action Indicated (NAI) · Lake Oswego, OR

Key facts

Inspection ID 869588
Firm BIOTRONIK Inc
FEI number 1028232
Address 6024 Jean Rd
City Lake Oswego
State OR
ZIP 97035
Country United States
Fiscal year 2014
Inspection end date Mar 7, 2014
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
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
  • 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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