# Oklahoma Blood Institute Norman Center, Norman, OK – FDA Inspections

Source: https://www.keypedia.com/companies/oklahoma-blood-institute-norman-center/03b16c22-d16c-4475-b45f-e33571a7ba6c

> Inspection records and compliance data for Oklahoma Blood Institute Norman Center in Norman, Oklahoma. 6 FDA inspections on record, 1 Form 483, last inspected February 28, 2023.

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## Details

- Name: Oklahoma Blood Institute Norman Center
- FEI Number: 3003949967
- Address Line 1: 1004 24th Ave Nw Ste 101
- City: Norman
- State: Oklahoma
- Zip Code: 73069
- Country Name: United States
- Address: 1004 24th Ave Nw Ste 101, Norman, Oklahoma 73069, United States
- Country: United States

## Related Documents

- FDA Inspection 1199398 - Oklahoma Blood Institute Norman Center - 2023-02-28 — classification: No Action Indicated (NAI), source: FDA, date: February 28, 2023
- FDA Inspection 1199398 - Oklahoma Blood Institute Norman Center - 2023-02-28 — classification: No Action Indicated (NAI), source: FDA, date: February 28, 2023
- [483 - Oklahoma Blood Institute Norman Center - 2019-03-22](https://www.keypedia.com/records/483/oklahoma-blood-institute-norman-center/63c0b9f9-7bca-4fc8-a9e0-e0e28a125cf7) — source: FDA, date: March 22, 2019
- [FDA Inspection 1084148 - Oklahoma Blood Institute Norman Center - 2019-03-22](https://www.keypedia.com/records/fda_inspections/oklahoma-blood-institute-norman-center/c4d128f5-9667-481d-a6fe-9da2238296c7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 22, 2019
- FDA Inspection 1013356 - Oklahoma Blood Institute Norman Center - 2017-05-25 — classification: No Action Indicated (NAI), source: FDA, date: May 25, 2017
- FDA Inspection 891511 - Oklahoma Blood Institute Norman Center - 2014-08-18 — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2014
- FDA Inspection 777900 - Oklahoma Blood Institute Norman Center - 2012-04-20 — classification: No Action Indicated (NAI), source: FDA, date: April 20, 2012
- FDA Inspection 651765 - Oklahoma Blood Institute Norman Center - 2010-03-03 — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2010

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