# Providence Health & Services Montana, Missoula, MT – FDA Inspections

Source: https://www.keypedia.com/companies/providence-health-services-montana/0e41934b-d5a2-412f-bc34-41bfbfa9fbcf

> Inspection records and compliance data for Providence Health & Services Montana in Missoula, Montana. 7 FDA inspections on record, last inspected August 06, 2025.

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## Details

- Name: Providence Health & Services Montana
- FEI Number: 1771624
- Address Line 1: 500 W Broadway St
- City: Missoula
- State: Montana
- Zip Code: 59802
- Country Name: United States
- Address: 500 W Broadway St, Missoula, Montana 59802, United States
- Country: United States

## Related Documents

- FDA Inspection 1280484 - Providence Health & Services Montana - 2025-08-06 — source: FDA, date: August 6, 2025
- FDA Inspection 1280484 - Providence Health & Services Montana - 2025-08-06 — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2025
- FDA Inspection 1215886 - Providence Health & Services Montana - 2023-07-27 — classification: No Action Indicated (NAI), source: FDA, date: July 27, 2023
- FDA Inspection 1064085 - Providence Health & Services Montana - 2018-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2018
- FDA Inspection 976157 - Providence Health & Services Montana - 2016-06-02 — classification: No Action Indicated (NAI), source: FDA, date: June 2, 2016
- [FDA Inspection 881174 - Providence Health & Services Montana - 2014-05-15](https://www.keypedia.com/records/fda_inspections/providence-health-services-montana/ed1e5ef9-c3f9-4688-b994-b350dfda9cca) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 15, 2014
- [FDA Inspection 799211 - Providence Health & Services Montana - 2012-09-12](https://www.keypedia.com/records/fda_inspections/providence-health-services-montana/64108e4b-c59c-4f5b-8d7c-999497744211) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 12, 2012
- FDA Inspection 673152 - Providence Health & Services Montana - 2010-07-20 — classification: No Action Indicated (NAI), source: FDA, date: July 20, 2010

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