# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/f54ecb4f-07ea-42b7-a5c3-dee609c98b1c

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

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## Details

- Name: OneBlood, Inc.
- FEI Number: 1035351
- City: Plantation
- State: Florida
- Country Name: United States
- Address Line 1: 1855 N Pine Island Rd
- Zip Code: 33322

## Related Documents

- [FDA Inspection 1155498 - OneBlood, Inc. - 2021-10-21](https://www.keypedia.com/records/fda_inspections/oneblood-inc/37467619-0b21-43a5-b8f8-499c57c71b7a) — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2021
- [FDA Inspection 1155498 - OneBlood, Inc. - 2021-10-21](https://www.keypedia.com/records/fda_inspections/oneblood-inc/ca83806a-1781-4108-8753-fd4b355f5639) — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2021
- [FDA Inspection 1078436 - OneBlood, Inc. - 2019-01-31](https://www.keypedia.com/records/fda_inspections/oneblood-inc/365580a4-cc67-46bb-9565-b1bd1e19267c) — classification: No Action Indicated (NAI), source: FDA, date: January 31, 2019
- [FDA Inspection 995160 - OneBlood, Inc. - 2016-12-06](https://www.keypedia.com/records/fda_inspections/oneblood-inc/b8020a6b-2926-4f9b-83aa-54811dae4f40) — classification: No Action Indicated (NAI), source: FDA, date: December 6, 2016
- [FDA Inspection 915100 - OneBlood, Inc. - 2015-02-23](https://www.keypedia.com/records/fda_inspections/oneblood-inc/951b97dc-992c-4777-bdff-7c649b9d6656) — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2015
- [FDA Inspection 821973 - OneBlood, Inc. - 2013-03-12](https://www.keypedia.com/records/fda_inspections/oneblood-inc/c043fe54-b2cc-4091-a1dd-beacf5e64822) — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2013
- [FDA Inspection 734632 - OneBlood, Inc. - 2011-07-14](https://www.keypedia.com/records/fda_inspections/oneblood-inc/0fcbe2c7-698c-468a-bbd7-15d5f3edb9a7) — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2011

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