# FDA Inspection 589006 - EKOS Corporation - May 19, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/ekos-corporation/73e2bc68-971a-426a-b5d2-e7c9125a2608
Source feed: FDA_Inspections

> FDA Inspection 589006 for EKOS Corporation on May 19, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 589006
- Company Name: EKOS Corporation
- Inspection Date: 2009-05-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/ekos-corporation/1b7ff204-434d-48c1-82c1-8b9b09d463ee

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