FDA inspection

Siemens Medical Solutions USA, Inc.: FDA inspection ending Jun 7, 2019

FDA inspection 1096686 · No Action Indicated (NAI) · Knoxville, TN

Key facts

Inspection ID 1096686
Firm Siemens Medical Solutions USA, Inc.
FEI number 1034973
Address 810 Innovation Dr
City Knoxville
State TN
ZIP 37932
Country United States
Fiscal year 2019
Inspection end date Jun 7, 2019
Classification No Action Indicated (NAI)
Project area Postmarket Assurance: 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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