# One Blood Inc, Charlotte, NC – FDA Inspections

Source: https://www.keypedia.com/companies/one-blood-inc/310228bb-fa51-4a71-a05e-0b9ffdc34343

> Inspection records and compliance data for One Blood Inc in Charlotte, North Carolina. 8 FDA inspections on record, last inspected September 11, 2025.

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## Details

- Name: One Blood Inc
- FEI Number: 3004054586
- Address Line 1: 700 Forest Point Cir
- City: Charlotte
- State: North Carolina
- Zip Code: 28273
- Country Name: United States
- Address: 700 Forest Point Cir, Charlotte, North Carolina 28273, United States
- Country: United States

## Related Documents

- FDA Inspection 1283848 - One Blood Inc - 2025-09-11 — source: FDA, date: September 11, 2025
- FDA Inspection 1283848 - One Blood Inc - 2025-09-11 — classification: No Action Indicated (NAI), source: FDA, date: September 11, 2025
- FDA Inspection 1192829 - One Blood Inc - 2022-11-30 — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2022
- [FDA Inspection 1192829 - One Blood Inc - 2022-11-30](https://www.keypedia.com/records/fda_inspections/one-blood-inc/c7a16a5c-93fb-4360-aff2-fffccfa700c0) — classification: No Action Indicated (NAI), source: FDA, date: November 30, 2022
- FDA Inspection 1091239 - One Blood Inc - 2019-05-17 — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2019
- FDA Inspection 1010313 - One Blood Inc - 2017-05-05 — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2017
- FDA Inspection 925358 - One Blood Inc - 2015-05-01 — classification: No Action Indicated (NAI), source: FDA, date: May 1, 2015
- FDA Inspection 828317 - One Blood Inc - 2013-04-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 12, 2013
- FDA Inspection 729133 - One Blood Inc - 2011-06-09 — classification: No Action Indicated (NAI), source: FDA, date: June 9, 2011
- [FDA Inspection 669204 - One Blood Inc - 2010-06-24](https://www.keypedia.com/records/fda_inspections/one-blood-inc/8b586b52-081f-47f0-839b-b532f331c8fa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 24, 2010

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