# Overton Brooks VA Medical Center, Shreveport, LA – FDA Inspections

Source: https://www.keypedia.com/companies/overton-brooks-va-medical-center/e0aaed00-95ee-4850-9429-20f0dee8b22d

> Inspection records and compliance data for Overton Brooks VA Medical Center in Shreveport, Louisiana. 2 FDA inspections on record (1 OAI), 2 Form 483s, last inspected December 18, 2024.

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## Details

- Name: Overton Brooks VA Medical Center
- FEI Number: 3013236711
- Facility Type: Producer of Sterile and Non-sterile Drug Products
- Address Line 1: 510 E Stoner Ave
- City: Shreveport
- State: Louisiana
- Zip Code: 71101
- Country Name: United States
- Address: 510 E Stoner Ave, Shreveport, Louisiana 71101, United States
- Country: United States

## Related Documents

- [483 - Overton Brooks VA Medical Center - 2024-12-18](https://www.keypedia.com/records/483/overton-brooks-va-medical-center/09d9357d-b5d5-4dee-bad7-f2a7699fdfe8) — source: FDA, date: December 18, 2024
- [FDA Inspection 1257010 - Overton Brooks VA Medical Center - 2024-12-18](https://www.keypedia.com/records/fda_inspections/overton-brooks-va-medical-center/ca9bc93d-9604-4ea4-838a-8018260747e2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 18, 2024
- [483 - Overton Brooks VA Medical Center - 2020-02-12](https://www.keypedia.com/records/483/overton-brooks-va-medical-center/863d56e1-7125-4837-a29b-c2abbd46a764) — source: FDA, date: February 12, 2020
- [483 - Overton Brooks VA Medical Center - 2020-02-03](https://www.keypedia.com/records/483/overton-brooks-va-medical-center/2dc6bd27-f163-470a-84ea-81e907734166) — source: FDA, date: February 3, 2020
- [483 - Overton Brooks VA Medical Center - 2017-02-17](https://www.keypedia.com/records/483/overton-brooks-va-medical-center/8f097a0b-5095-4195-9a5b-d3e73f0632ff) — source: FDA, date: February 17, 2017
- [FDA Inspection 1002344 - Overton Brooks VA Medical Center - 2017-02-17](https://www.keypedia.com/records/fda_inspections/overton-brooks-va-medical-center/495b1c55-1426-4e9a-92ef-5a1e87748965) — classification: Official Action Indicated (OAI), source: FDA, date: February 17, 2017

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