# FDA Inspection 1050573 - XVIVO Perfusion, Inc - May 03, 2018

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

> FDA Inspection 1050573 for XVIVO Perfusion, Inc on May 03, 2018. Classification: No Action Indicated (NAI).

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## Details

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

## Related Documents

- [FDA Inspection 1064057 - 2018-08-30](https://www.globalkeysolutions.net/records/fda_inspections/xvivo-perfusion-inc/9265614c-2660-4580-99f3-70c123bef58e)
- [FDA Inspection 1050573 - 2018-05-03](https://www.globalkeysolutions.net/records/fda_inspections/xvivo-perfusion-inc/4e163933-8dea-4f1d-ae3e-5a0b59a26cb6)

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

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