# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/18cbbedf-c422-44f8-8007-af8fa80bec85

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

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## Details

- Name: OneBlood, Inc.
- FEI Number: 1072594
- City: Hialeah
- State: Florida
- Country Name: United States
- Address Line 1: 8101 W 26th Ave
- Zip Code: 33016

## Related Documents

- [FDA Inspection 1221558 - OneBlood, Inc. - 2023-10-24](https://www.keypedia.com/records/fda_inspections/oneblood-inc/a4abc150-4b16-4f85-b8f7-7d00bcec137e) — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2023
- [FDA Inspection 1155113 - OneBlood, Inc. - 2021-11-04](https://www.keypedia.com/records/fda_inspections/oneblood-inc/6fdd71b8-f28e-4501-93c8-36f0db8ded77) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2021
- [FDA Inspection 1155113 - OneBlood, Inc. - 2021-11-04](https://www.keypedia.com/records/fda_inspections/oneblood-inc/a0e884e9-8e19-4afb-9cd3-1212e165e80a) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2021
- [FDA Inspection 1100052 - OneBlood, Inc. - 2019-07-30](https://www.keypedia.com/records/fda_inspections/oneblood-inc/5cbfbc23-beac-49a2-889b-f05d0ed173d3) — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2019
- [FDA Inspection 1027412 - OneBlood, Inc. - 2017-08-24](https://www.keypedia.com/records/fda_inspections/oneblood-inc/1a03d6d8-84ac-4c17-9ebd-6012dbf4b4bc) — classification: No Action Indicated (NAI), source: FDA, date: August 24, 2017
- [FDA Inspection 947063 - OneBlood, Inc. - 2015-10-09](https://www.keypedia.com/records/fda_inspections/oneblood-inc/1416ce7a-15ea-4e17-bc82-69f518a02df4) — classification: No Action Indicated (NAI), source: FDA, date: October 9, 2015
- [FDA Inspection 843007 - OneBlood, Inc. - 2013-08-02](https://www.keypedia.com/records/fda_inspections/oneblood-inc/9fb98fba-632e-45de-a501-a04bc8c0c17e) — classification: No Action Indicated (NAI), source: FDA, date: August 2, 2013

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