# Department of Defense - Army Robertson Blood Center Ft Leonard Wood, Fort Leonard Wood, MO – FDA Inspections

Source: https://www.keypedia.com/companies/department-of-defense-army-robertson-blood-center-ft-leonard-wood/490dcf7a-e4ac-42ed-bed7-1ac3121c091c

> Inspection records and compliance data for Department of Defense - Army Robertson Blood Center Ft Leonard Wood in Fort Leonard Wood, Missouri. 7 FDA inspections on record, last inspected July 19, 2024.

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## Details

- Name: Department of Defense - Army Robertson Blood Center Ft Leonard Wood
- FEI Number: 3006385466
- Address Line 1: 6261 Buckeye Ave, Bldg 759
- City: Fort Leonard Wood
- State: Missouri
- Zip Code: 65473
- Country Name: United States
- Address: 6261 Buckeye Ave, Bldg 759, Fort Leonard Wood, Missouri 65473, United States
- Country: United States

## Related Documents

- FDA Inspection 1247307 - Department of Defense - Army Robertson Blood Center Ft Leonard Wood - 2024-07-19 — classification: No Action Indicated (NAI), source: FDA, date: July 19, 2024
- FDA Inspection 1084846 - Department of Defense - Army Robertson Blood Center Ft Leonard Wood - 2019-03-26 — classification: No Action Indicated (NAI), source: FDA, date: March 26, 2019
- FDA Inspection 1008991 - Department of Defense - Army Robertson Blood Center Ft Leonard Wood - 2017-03-28 — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2017
- FDA Inspection 922280 - Department of Defense - Army Robertson Blood Center Ft Leonard Wood - 2015-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2015
- FDA Inspection 842386 - Department of Defense - Army Robertson Blood Center Ft Leonard Wood - 2013-07-29 — classification: No Action Indicated (NAI), source: FDA, date: July 29, 2013
- FDA Inspection 720355 - Department of Defense - Army Robertson Blood Center Ft Leonard Wood - 2011-04-13 — classification: No Action Indicated (NAI), source: FDA, date: April 13, 2011
- FDA Inspection 615064 - Department of Defense - Army Robertson Blood Center Ft Leonard Wood - 2009-09-23 — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2009

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