# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/a0d57be8-29f0-4fcf-8bcc-921df8547cd1

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

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## Details

- Name: OneBlood, Inc.
- FEI Number: 1000143701
- City: Stuart
- State: Florida
- Country Name: United States
- Address Line 1: 2229 SE Ocean Blvd
- Zip Code: 34996

## Related Documents

- [FDA Inspection 1224938 - OneBlood, Inc. - 2023-12-07](https://www.keypedia.com/records/fda_inspections/oneblood-inc/b3ef3ca8-8df0-4d14-b75e-41dbdd56b1a9) — classification: No Action Indicated (NAI), source: FDA, date: December 7, 2023
- [FDA Inspection 1100466 - OneBlood, Inc. - 2019-07-11](https://www.keypedia.com/records/fda_inspections/oneblood-inc/41b98d85-3591-4c34-afc2-b2dda4a9f879) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2019
- [FDA Inspection 1013827 - OneBlood, Inc. - 2017-03-17](https://www.keypedia.com/records/fda_inspections/oneblood-inc/13d56849-2eb3-4311-b4b3-59319ac961b8) — classification: No Action Indicated (NAI), source: FDA, date: March 17, 2017
- [FDA Inspection 917054 - OneBlood, Inc. - 2015-03-06](https://www.keypedia.com/records/fda_inspections/oneblood-inc/7c539ca1-b0e2-4daf-8524-4b766f81ca06) — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2015
- [FDA Inspection 841117 - OneBlood, Inc. - 2013-07-22](https://www.keypedia.com/records/fda_inspections/oneblood-inc/5a6915a3-7993-4f42-846b-627c8f99bddf) — classification: No Action Indicated (NAI), source: FDA, date: July 22, 2013
- [FDA Inspection 731985 - OneBlood, Inc. - 2011-06-28](https://www.keypedia.com/records/fda_inspections/oneblood-inc/79a70e85-7a78-4145-9307-f7f00a7a8762) — classification: No Action Indicated (NAI), source: FDA, date: June 28, 2011
- [FDA Inspection 558205 - OneBlood, Inc. - 2009-01-22](https://www.keypedia.com/records/fda_inspections/oneblood-inc/a1ced014-7b13-4f17-b863-1096ce68e704) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2009

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