# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/28b52c38-ac03-4005-90fc-45553ec9212c

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

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## Details

- Name: OneBlood, Inc.
- FEI Number: 1070214
- City: Palm Beach Gardens
- State: Florida
- Country Name: United States
- Address Line 1: 3451 Northlake Blvd
- Zip Code: 33403

## Related Documents

- [FDA Inspection 1205042 - OneBlood, Inc. - 2023-05-10](https://www.keypedia.com/records/fda_inspections/oneblood-inc/cc19a781-3e39-44ef-a802-d0d1c48f7e55) — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2023
- [FDA Inspection 1101215 - OneBlood, Inc. - 2019-07-17](https://www.keypedia.com/records/fda_inspections/oneblood-inc/8b7298f0-919e-4477-95d7-695047c14f62) — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2019
- [FDA Inspection 1027468 - OneBlood, Inc. - 2017-08-24](https://www.keypedia.com/records/fda_inspections/oneblood-inc/759d1942-3d70-4e24-9015-d092af805180) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 24, 2017
- [FDA Inspection 942737 - OneBlood, Inc. - 2015-09-18](https://www.keypedia.com/records/fda_inspections/oneblood-inc/906ceb24-94bc-49d5-9392-db54621dc5e0) — classification: No Action Indicated (NAI), source: FDA, date: September 18, 2015
- [FDA Inspection 843950 - OneBlood, Inc. - 2013-08-09](https://www.keypedia.com/records/fda_inspections/oneblood-inc/0a572083-b265-441e-87f4-d1088ae78a10) — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2013
- [FDA Inspection 741259 - OneBlood, Inc. - 2011-08-25](https://www.keypedia.com/records/fda_inspections/oneblood-inc/adb0f1f4-c8bc-4a48-b631-2c61f093383e) — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2011
- [FDA Inspection 579642 - OneBlood, Inc. - 2009-04-24](https://www.keypedia.com/records/fda_inspections/oneblood-inc/769adf63-0ce0-4c33-8157-c500adaccf3e) — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2009

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