# XVIVO Perfusion, Inc – FDA Inspection, May 3, 2018

Source: https://www.keypedia.com/records/fda_inspections/xvivo-perfusion-inc/67130f52-d7fa-4cc3-9cda-51d1567e4f14
Source feed: FDA_Inspections

> FDA inspection 1050573 of XVIVO Perfusion, Inc, May 03, 2018. Classification: No Action Indicated (NAI). 4 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1050573
- Company Name: XVIVO Perfusion, Inc
- Inspection Date: 2018-05-03
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1064057 - 2018-08-30](https://www.keypedia.com/records/fda_inspections/xvivo-perfusion-inc/bebcc997-0ecd-4787-a410-418d215c9da9)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/christine-i-shaw/480cb61e-f173-432d-b84a-c8b492192302)

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