# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/4814b4d1-2b15-4e4e-a2e6-7f2900885fcc

> Inspection records and compliance data for OneBlood, Inc. in Melbourne, Florida. Access full analysis and detailed observations.

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## Details

- Name: OneBlood, Inc.
- FEI Number: 1000143757
- City: Melbourne
- State: Florida
- Country Name: United States
- Address Line 1: 789 S Babcock St Ste 127
- Zip Code: 32901

## Related Documents

- [FDA Inspection 1230725 - OneBlood, Inc. - 2024-02-15](https://www.keypedia.com/records/fda_inspections/oneblood-inc/2fa12d68-8fad-4dc7-8917-962353d7c623) — classification: No Action Indicated (NAI), source: FDA, date: February 15, 2024
- [FDA Inspection 1088840 - OneBlood, Inc. - 2019-05-02](https://www.keypedia.com/records/fda_inspections/oneblood-inc/7f12cc84-3742-42e4-b8e0-6e734a48e269) — classification: No Action Indicated (NAI), source: FDA, date: May 2, 2019
- [FDA Inspection 1012420 - OneBlood, Inc. - 2017-04-04](https://www.keypedia.com/records/fda_inspections/oneblood-inc/8603d37e-5358-443f-992a-be901a70aab9) — classification: No Action Indicated (NAI), source: FDA, date: April 4, 2017
- [FDA Inspection 940840 - OneBlood, Inc. - 2015-09-03](https://www.keypedia.com/records/fda_inspections/oneblood-inc/2d40e8a3-efca-4623-aae1-37ea34d9cec2) — classification: No Action Indicated (NAI), source: FDA, date: September 3, 2015
- [FDA Inspection 822984 - OneBlood, Inc. - 2013-03-08](https://www.keypedia.com/records/fda_inspections/oneblood-inc/89e42b40-33f1-4e9f-b77f-a30f0b86f600) — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2013
- [FDA Inspection 703057 - OneBlood, Inc. - 2010-12-23](https://www.keypedia.com/records/fda_inspections/oneblood-inc/10b8df60-583b-4450-97eb-28159e80b1bc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 23, 2010
- [FDA Inspection 550031 - OneBlood, Inc. - 2008-12-05](https://www.keypedia.com/records/fda_inspections/oneblood-inc/2084c080-d511-4588-9d7b-2973bcf87d48) — classification: No Action Indicated (NAI), source: FDA, date: December 5, 2008

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