# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/acafb8ec-46ce-4ab6-ae18-e1c772eb2e7b

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

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## Details

- Name: OneBlood, Inc.
- FEI Number: 3005909376
- City: Clermont
- State: Florida
- Country Name: United States
- Address Line 1: 1200 Oakley Seaver Dr Ste 106
- Zip Code: 34711

## Related Documents

- [FDA Inspection 1221537 - OneBlood, Inc. - 2023-10-25](https://www.keypedia.com/records/fda_inspections/oneblood-inc/5aef74cd-ff40-4eff-b5ad-b943f091ad30) — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2023
- [FDA Inspection 1106325 - OneBlood, Inc. - 2019-09-17](https://www.keypedia.com/records/fda_inspections/oneblood-inc/8e8ac0fb-4364-430b-99e5-ec59ffd74b87) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2019
- [FDA Inspection 1028880 - OneBlood, Inc. - 2017-09-20](https://www.keypedia.com/records/fda_inspections/oneblood-inc/81784fc8-0147-4b5d-9ac3-06935df574c0) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2017
- [FDA Inspection 948671 - OneBlood, Inc. - 2015-11-18](https://www.keypedia.com/records/fda_inspections/oneblood-inc/ba064330-947f-4e63-b044-653cd7d4391b) — classification: No Action Indicated (NAI), source: FDA, date: November 18, 2015
- [FDA Inspection 862941 - OneBlood, Inc. - 2014-01-22](https://www.keypedia.com/records/fda_inspections/oneblood-inc/810ecfe8-dfc6-4c74-9718-51c3bcebff1a) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2014
- [FDA Inspection 751936 - OneBlood, Inc. - 2011-10-25](https://www.keypedia.com/records/fda_inspections/oneblood-inc/8350c01a-5886-4b8b-ac3a-4c60c5d690ca) — classification: No Action Indicated (NAI), source: FDA, date: October 25, 2011
- [FDA Inspection 634591 - OneBlood, Inc. - 2009-12-10](https://www.keypedia.com/records/fda_inspections/oneblood-inc/f2034f47-e5df-4198-af12-9eaa5600d3b8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 10, 2009

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