# FDA Inspection 1057926 - ReNovo, Inc. - June 21, 2018

Source: https://www.keypedia.com/records/fda_inspections/renovo-inc/33862b6c-a538-4b77-aafd-9c60105aeb99
Source feed: FDA_Inspections

> FDA Inspection 1057926 for ReNovo, Inc. on June 21, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1057926
- Company Name: ReNovo, Inc.
- Inspection Date: 2018-06-21
- 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/renovo-inc/05b78813-dfe4-488e-b1f9-624731d7205d

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