# Department of Defense - Army, Fort Leonard Wood, MO – FDA Inspections

Source: https://www.keypedia.com/companies/department-of-defense-army/93cfe484-b2d8-4b49-82df-c67b9c05501f

> Inspection records and compliance data for Department of Defense - Army in Fort Leonard Wood, Missouri. 7 FDA inspections on record, 1 Form 483, last inspected July 16, 2024.

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## Details

- Name: Department of Defense - Army
- FEI Number: 1978003
- Address Line 1: General Leonard Wood Army Community Hospital, 126 Missouri Ave
- City: Fort Leonard Wood
- State: Missouri
- Zip Code: 65473
- Country Name: United States
- Address: General Leonard Wood Army Community Hospital, 126 Missouri Ave, Fort Leonard Wood, Missouri 65473, United States
- Country: United States

## Related Documents

- FDA Inspection 1246935 - Department of Defense - Army - 2024-07-16 — classification: No Action Indicated (NAI), source: FDA, date: July 16, 2024
- FDA Inspection 1084839 - Department of Defense - Army - 2019-03-21 — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2019
- [FDA Inspection 1009238 - Department of Defense - Army - 2017-03-31](https://www.keypedia.com/records/fda_inspections/department-of-defense-army/79ac5d95-643a-40e9-b108-3fc0d2870f66) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2017
- FDA Inspection 922990 - Department of Defense - Army - 2015-04-16 — classification: No Action Indicated (NAI), source: FDA, date: April 16, 2015
- FDA Inspection 842388 - Department of Defense - Army - 2013-07-30 — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2013
- FDA Inspection 842388 - Department of Defense - Army - 2013-07-30 — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2013
- FDA Inspection 720351 - Department of Defense - Army - 2011-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2011
- FDA Inspection 615046 - Department of Defense - Army - 2009-09-23 — classification: No Action Indicated (NAI), source: FDA, date: September 23, 2009

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