# FDA Inspection 1097120 - Ekso Bionics - June 28, 2019

Source: https://www.keypedia.com/records/fda_inspections/ekso-bionics/48108ff6-68b2-44ca-8d35-0892c18896be
Source feed: FDA_Inspections

> FDA Inspection 1097120 for Ekso Bionics on June 28, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097120
- Company Name: Ekso Bionics
- Inspection Date: 2019-06-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/ekso-bionics/2dd52747-89f9-4922-b0a5-24462e168ca2

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7