# FDA Inspection 939291 - CardioQuip, LLC - August 28, 2015

Source: https://www.keypedia.com/records/fda_inspections/cardioquip-llc/2fc623eb-ae90-46bf-8900-38cfa96ef5d0
Source feed: FDA_Inspections

> FDA Inspection 939291 for CardioQuip, LLC on August 28, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939291
- Company Name: CardioQuip, LLC
- Inspection Date: 2015-08-28
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/cardioquip-llc/fc77f9cb-e6a5-495b-8930-55ccd8a5dee6

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