# FDA Inspection 974115 - Rhythmedix - May 27, 2016

Source: https://www.keypedia.com/records/fda_inspections/rhythmedix/4315e81e-4917-4b5a-b3a1-dfc8c1f5a196
Source feed: FDA_Inspections

> FDA Inspection 974115 for Rhythmedix on May 27, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 974115
- Company Name: Rhythmedix
- Inspection Date: 2016-05-27
- Classification: Voluntary Action Indicated (VAI)
- 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/rhythmedix/f8cc6eed-1da1-46bd-a25a-d71bc1dcc909

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