# John J. Pershing Veterans Administration Medical Center, Poplar Bluff, MO – FDA Inspections

Source: https://www.keypedia.com/companies/john-j-pershing-veterans-administration-medical-center/86afddd5-cc1c-4b02-81dc-2a74f59afee3

> Inspection records and compliance data for John J. Pershing Veterans Administration Medical Center in Poplar Bluff, Missouri. 7 FDA inspections on record, last inspected July 17, 2025.

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## Details

- Name: John J. Pershing Veterans Administration Medical Center
- FEI Number: 1971618
- Address Line 1: 1500 N Westwood Blvd
- City: Poplar Bluff
- State: Missouri
- Zip Code: 63901
- Country Name: United States
- Address: 1500 N Westwood Blvd, Poplar Bluff, Missouri 63901, United States
- Country: United States

## Related Documents

- FDA Inspection 1277049 - John J. Pershing Veterans Administration Medical Center - 2025-07-17 — source: FDA, date: July 17, 2025
- FDA Inspection 1277049 - John J. Pershing Veterans Administration Medical Center - 2025-07-17 — classification: No Action Indicated (NAI), source: FDA, date: July 17, 2025
- FDA Inspection 1203767 - John J. Pershing Veterans Administration Medical Center - 2023-04-18 — classification: No Action Indicated (NAI), source: FDA, date: April 18, 2023
- FDA Inspection 1063910 - John J. Pershing Veterans Administration Medical Center - 2018-08-22 — classification: No Action Indicated (NAI), source: FDA, date: August 22, 2018
- FDA Inspection 946076 - John J. Pershing Veterans Administration Medical Center - 2015-10-21 — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2015
- FDA Inspection 861991 - John J. Pershing Veterans Administration Medical Center - 2014-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2014
- FDA Inspection 784222 - John J. Pershing Veterans Administration Medical Center - 2012-05-29 — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2012
- FDA Inspection 666700 - John J. Pershing Veterans Administration Medical Center - 2010-05-18 — classification: No Action Indicated (NAI), source: FDA, date: May 18, 2010

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