# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/df0ecb37-ca74-402c-8059-b0912eb8ec18

> Inspection records and compliance data for OneBlood, Inc. in Saint Marys, Georgia. Access full analysis and detailed observations.

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## Details

- Name: OneBlood, Inc.
- FEI Number: 3001619959
- City: Saint Marys
- State: Georgia
- Country Name: United States
- Address Line 1: 6586 Ga Highway 40 E Ste A21
- Zip Code: 31558

## Related Documents

- [FDA Inspection 1146343 - OneBlood, Inc. - 2021-07-06](https://www.keypedia.com/records/fda_inspections/oneblood-inc/166ada19-24b2-4c90-9aa7-bc9404379138) — classification: No Action Indicated (NAI), source: FDA, date: July 6, 2021
- [FDA Inspection 1146343 - OneBlood, Inc. - 2021-07-06](https://www.keypedia.com/records/fda_inspections/oneblood-inc/8352bcbf-3186-4a19-b023-3500083f018e) — classification: No Action Indicated (NAI), source: FDA, date: July 6, 2021
- [FDA Inspection 1064443 - OneBlood, Inc. - 2018-06-12](https://www.keypedia.com/records/fda_inspections/oneblood-inc/c0977dbe-f590-4b69-9384-68cef3a6e15e) — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2018
- [FDA Inspection 969054 - OneBlood, Inc. - 2016-04-29](https://www.keypedia.com/records/fda_inspections/oneblood-inc/79b6eea7-c053-42d7-823f-a763a1643754) — classification: No Action Indicated (NAI), source: FDA, date: April 29, 2016
- [FDA Inspection 891164 - OneBlood, Inc. - 2014-08-13](https://www.keypedia.com/records/fda_inspections/oneblood-inc/0f853b2d-3130-461c-a48a-ee430e486d99) — classification: No Action Indicated (NAI), source: FDA, date: August 13, 2014
- [FDA Inspection 798128 - OneBlood, Inc. - 2012-09-11](https://www.keypedia.com/records/fda_inspections/oneblood-inc/bc91c919-a9aa-416e-8c92-523a52d8caf1) — classification: No Action Indicated (NAI), source: FDA, date: September 11, 2012
- [FDA Inspection 651234 - OneBlood, Inc. - 2010-03-11](https://www.keypedia.com/records/fda_inspections/oneblood-inc/b8a9f560-2d44-4a5f-843f-fb94b277e8b7) — classification: No Action Indicated (NAI), source: FDA, date: March 11, 2010

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