FDA inspection

Ekso Bionics: FDA inspection ending Sep 11, 2015

FDA inspection 946397 · Voluntary Action Indicated (VAI) · San Rafael, CA

Key facts

Inspection ID 946397
Firm Ekso Bionics
FEI number 3009495988
Address 1414 Harbour Way S Ste 1201
City San Rafael
State CA
ZIP 94901
Country United States
Fiscal year 2015
Inspection end date Sep 11, 2015
Classification Voluntary Action Indicated (VAI)
Project area Bioresearch Monitoring
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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