# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/10fac2bb-ec38-41d9-b5c8-bdde9154f08a

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

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## Details

- Name: OneBlood, Inc.
- FEI Number: 3006255520
- City: North Port
- State: Florida
- Country Name: United States
- Address Line 1: 14820 Tamiami Trl
- Zip Code: 34287

## Related Documents

- [FDA Inspection 1233178 - OneBlood, Inc. - 2024-05-07](https://www.keypedia.com/records/fda_inspections/oneblood-inc/548f983f-dcea-4178-b871-ff1a0a3f9236) — classification: No Action Indicated (NAI), source: FDA, date: May 7, 2024
- [FDA Inspection 1085331 - OneBlood, Inc. - 2019-03-27](https://www.keypedia.com/records/fda_inspections/oneblood-inc/13433045-935f-4dfc-a99c-1b1cc4406edc) — classification: No Action Indicated (NAI), source: FDA, date: March 27, 2019
- [FDA Inspection 995028 - OneBlood, Inc. - 2016-12-15](https://www.keypedia.com/records/fda_inspections/oneblood-inc/3a859752-79e7-4cf1-8862-fb7c4b2a00df) — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2016
- [FDA Inspection 899977 - OneBlood, Inc. - 2014-10-16](https://www.keypedia.com/records/fda_inspections/oneblood-inc/d2a76a9d-c593-4885-bdea-f02310873778) — classification: No Action Indicated (NAI), source: FDA, date: October 16, 2014
- [FDA Inspection 816366 - OneBlood, Inc. - 2013-01-30](https://www.keypedia.com/records/fda_inspections/oneblood-inc/6b8ab965-1092-4d57-81e6-bb3afa61c04e) — classification: No Action Indicated (NAI), source: FDA, date: January 30, 2013
- [FDA Inspection 721718 - OneBlood, Inc. - 2011-04-26](https://www.keypedia.com/records/fda_inspections/oneblood-inc/01808213-94c8-49b8-ab49-1f13b8f96d62) — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2011
- [FDA Inspection 583182 - OneBlood, Inc. - 2009-05-12](https://www.keypedia.com/records/fda_inspections/oneblood-inc/30291067-e67e-4bb2-a08d-3abe5b01a7c5) — classification: No Action Indicated (NAI), source: FDA, date: May 12, 2009

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