FDA inspection

Arstasis, Inc: FDA inspection ending Mar 16, 2011

FDA inspection 712648 · Voluntary Action Indicated (VAI) · Fremont, CA

Key facts

Inspection ID 712648
Firm Arstasis, Inc
FEI number 3008493244
Address 6500 Kaiser Dr Ste 120
City Fremont
State CA
ZIP 94555
Country United States
Fiscal year 2011
Inspection end date Mar 16, 2011
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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