FDA inspection

Siemens Healthcare Diagnostics: FDA inspection ending Jan 12, 2011

FDA inspection 705533 · No Action Indicated (NAI) · Los Angeles, CA

Key facts

Inspection ID 705533
Firm Siemens Healthcare Diagnostics
FEI number 3005250747
Address 5210 Pacific Concourse Dr
City Los Angeles
State CA
ZIP 90045
Country United States
Fiscal year 2011
Inspection end date Jan 12, 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
  • 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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