FDA inspection

Siemans Medial Solutions USA, Inc: FDA inspection ending May 22, 2015

FDA inspection 975916 · Voluntary Action Indicated (VAI) · Plymouth Meeting, PA

Key facts

Inspection ID 975916
Firm Siemans Medial Solutions USA, Inc
FEI number 3002626007
Address 5168 Campus Dr
City Plymouth Meeting
State PA
ZIP 19462-1123
Fiscal year 2015
Inspection end date May 22, 2015
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 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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