# OneBlood, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/oneblood-inc/ebef80ff-0b98-4c0b-8d06-4d3a1a2538f8

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

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## Details

- Name: OneBlood, Inc.
- FEI Number: 1052376
- City: Zephyrhills
- State: Florida
- Country Name: United States
- Address Line 1: 38040 Market Square Dr
- Zip Code: 33542

## Related Documents

- [FDA Inspection 1159820 - OneBlood, Inc. - 2021-12-10](https://www.keypedia.com/records/fda_inspections/oneblood-inc/a524129c-de98-4321-bf71-4ca174391f13) — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2021
- [FDA Inspection 1159820 - OneBlood, Inc. - 2021-12-10](https://www.keypedia.com/records/fda_inspections/oneblood-inc/1e13908a-29d6-4afe-8008-8d4d3afbde93) — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2021
- [FDA Inspection 1048999 - OneBlood, Inc. - 2018-03-02](https://www.keypedia.com/records/fda_inspections/oneblood-inc/7cd0bf71-0629-47fa-84c4-4a8af2071edb) — classification: No Action Indicated (NAI), source: FDA, date: March 2, 2018
- [FDA Inspection 980163 - OneBlood, Inc. - 2016-01-26](https://www.keypedia.com/records/fda_inspections/oneblood-inc/6fc573d7-8d12-406b-a569-f611fd6bafbd) — classification: No Action Indicated (NAI), source: FDA, date: January 26, 2016
- [FDA Inspection 887104 - OneBlood, Inc. - 2014-07-14](https://www.keypedia.com/records/fda_inspections/oneblood-inc/f4ab7aa2-7f54-4f12-9967-6f24365c3986) — classification: No Action Indicated (NAI), source: FDA, date: July 14, 2014
- [FDA Inspection 789411 - OneBlood, Inc. - 2012-07-06](https://www.keypedia.com/records/fda_inspections/oneblood-inc/35d22afd-2c33-4c04-a241-b124e92746f0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 6, 2012
- [FDA Inspection 663402 - OneBlood, Inc. - 2010-05-25](https://www.keypedia.com/records/fda_inspections/oneblood-inc/b001692a-f274-49a3-a7d4-a11d2526de8a) — classification: No Action Indicated (NAI), source: FDA, date: May 25, 2010

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