# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/87b15831-cef7-4285-af76-2c57e453071b

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

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## Details

- Name: OneBlood, Inc.
- FEI Number: 1036005
- City: Sebring
- State: Florida
- Country Name: United States
- Address Line 1: 6550 US Highway 27 N
- Zip Code: 33870

## Related Documents

- [FDA Inspection 1239971 - OneBlood, Inc. - 2024-05-09](https://www.keypedia.com/records/fda_inspections/oneblood-inc/d367e6bf-003c-4a40-8be0-0d816d93c5d4) — classification: No Action Indicated (NAI), source: FDA, date: May 9, 2024
- [FDA Inspection 1098298 - OneBlood, Inc. - 2019-06-12](https://www.keypedia.com/records/fda_inspections/oneblood-inc/0d9604b7-e7b2-4346-80e8-89576dee4eba) — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2019
- [FDA Inspection 1003268 - OneBlood, Inc. - 2017-01-19](https://www.keypedia.com/records/fda_inspections/oneblood-inc/80e777a5-a451-4629-b828-c9d2ad0b783d) — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2017
- [FDA Inspection 923097 - OneBlood, Inc. - 2015-04-21](https://www.keypedia.com/records/fda_inspections/oneblood-inc/0c06cce4-ebd6-40de-8ea3-95b6bce05925) — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2015
- [FDA Inspection 826248 - OneBlood, Inc. - 2013-04-03](https://www.keypedia.com/records/fda_inspections/oneblood-inc/132bd30b-e7ed-4cba-96e9-d74881093627) — classification: No Action Indicated (NAI), source: FDA, date: April 3, 2013
- [FDA Inspection 745933 - OneBlood, Inc. - 2011-09-22](https://www.keypedia.com/records/fda_inspections/oneblood-inc/40c357d7-f3e7-48fb-9a47-a69192ffb3b0) — classification: No Action Indicated (NAI), source: FDA, date: September 22, 2011
- [FDA Inspection 630227 - OneBlood, Inc. - 2009-11-24](https://www.keypedia.com/records/fda_inspections/oneblood-inc/02e3eb31-ae56-4660-9d0d-89694eefa06b) — classification: No Action Indicated (NAI), source: FDA, date: November 24, 2009

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