# FDA Inspection 1085127 - OneBlood, Inc. - April 02, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/oneblood-inc/db8f7fdb-025e-4313-ba9b-d29b92e33311
Source feed: FDA_Inspections

> FDA Inspection 1085127 for OneBlood, Inc. on April 02, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1085127
- Company Name: OneBlood, Inc.
- Inspection Date: 2019-04-02
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1229791 - 2024-06-10](https://www.globalkeysolutions.net/records/fda_inspections/oneblood-inc/8fd99486-5b44-4dc8-b32d-18fd1020855d)
- [FDA Inspection 1085127 - 2019-04-02](https://www.globalkeysolutions.net/records/fda_inspections/oneblood-inc/a83f0d13-4ea2-4a01-ad6a-ef37e1e3cf4b)
- [FDA Inspection 1085127 - 2019-04-02](https://www.globalkeysolutions.net/records/fda_inspections/oneblood-inc/61e1f2a7-abc5-44d5-80d3-929b5beea7a2)
- [FDA Inspection 985555 - 2016-08-12](https://www.globalkeysolutions.net/records/fda_inspections/oneblood-inc/46dbbdd5-1afc-47c8-9da5-3c1925fd8691)
- [FDA Inspection 985555 - 2016-08-12](https://www.globalkeysolutions.net/records/fda_inspections/oneblood-inc/32785041-e3fb-499d-bd02-e672c8c6a2a7)

Company: https://www.globalkeysolutions.net/companies/oneblood-inc/79fab388-8638-45e8-9ea6-ca699ba36a75

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