# FDA Inspection 993139 - Cardiokinetix Inc - November 17, 2016

Source: https://www.keypedia.com/records/fda_inspections/cardiokinetix-inc/efe7adaf-3a22-4a96-a155-8d721903a1a9
Source feed: FDA_Inspections

> FDA Inspection 993139 for Cardiokinetix Inc on November 17, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993139
- Company Name: Cardiokinetix Inc
- Inspection Date: 2016-11-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/cardiokinetix-inc/5c48135b-22e9-42eb-b6c1-6e22f5c8e1dc

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