FDA inspection

Elekta, Inc.: FDA inspection ending Nov 21, 2011

FDA inspection 753194 · Voluntary Action Indicated (VAI) · Sunnyvale, CA

Key facts

Inspection ID 753194
Firm Elekta, Inc.
FEI number 1000123805
Address 100 Mathilda Pl, 5th Floor
City Sunnyvale
State CA
ZIP 94086
Country United States
Fiscal year 2012
Inspection end date Nov 21, 2011
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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