# XVIVO Perfusion, Inc – FDA Inspection, Aug 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/xvivo-perfusion-inc/bebcc997-0ecd-4787-a410-418d215c9da9
Source feed: FDA_Inspections

> FDA inspection 1064057 of XVIVO Perfusion, Inc, August 30, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064057
- Company Name: XVIVO Perfusion, Inc
- Inspection Date: 2018-08-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1050573 - 2018-05-03](https://www.keypedia.com/records/fda_inspections/xvivo-perfusion-inc/67130f52-d7fa-4cc3-9cda-51d1567e4f14)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jonathan-r-campos/f4c6aba7-d0fe-43d2-95ae-5eb86a6659a4)

Company: https://www.keypedia.com/companies/xvivo-perfusion-inc/e5ca5b11-19c3-4b32-8f25-1aeccd82aaa9

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