FDA inspection

PULSION MEDICAL SYSTEMS SE: FDA inspection ending Jun 9, 2011

FDA inspection 731959 · No Action Indicated (NAI) · Feldkirchen

Key facts

Inspection ID 731959
Firm PULSION MEDICAL SYSTEMS SE
FEI number 3003263092
Address 81829, Joseph-Wild-Str. 20
City Feldkirchen
Country Germany
Fiscal year 2011
Inspection end date Jun 9, 2011
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

Browse all FDA inspections