# FDA Inspection 1027273 - Hemolife Medical Inc - August 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/hemolife-medical-inc/07f4e9dc-f50c-4e61-ac3c-b5e0fcef0b6a
Source feed: FDA_Inspections

> FDA Inspection 1027273 for Hemolife Medical Inc on August 18, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1027273
- Company Name: Hemolife Medical Inc
- Inspection Date: 2017-08-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/hemolife-medical-inc/ee01d2ec-ac14-4151-8b22-13e39765f6ea

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