# Inovise Medical, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/inovise-medical-inc/fd7e0066-9c0e-49fb-9bcf-e52d57df4102

> Inspection records and compliance data for Inovise Medical, Inc. in Beaverton, Oregon. Access full analysis and detailed observations.

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## Details

- Name: Inovise Medical, Inc.
- FEI Number: 3003264460
- City: Beaverton
- State: Oregon
- Country Name: United States
- Address Line 1: 8770 SW Nimbus Ave Ste D
- Zip Code: 97008

## Related Documents

- [FDA Inspection 933856 - Inovise Medical, Inc. - 2015-06-12](https://www.globalkeysolutions.net/records/fda_inspections/inovise-medical-inc/f8635936-2b0f-48c4-b74e-81adb7e53531) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 12, 2015
- [FDA Inspection 933856 - Inovise Medical, Inc. - 2015-06-12](https://www.globalkeysolutions.net/records/fda_inspections/inovise-medical-inc/ff4e4e75-12db-4a32-af8f-1ffad68da643) — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2015
- [FDA Inspection 823440 - Inovise Medical, Inc. - 2013-03-21](https://www.globalkeysolutions.net/records/fda_inspections/inovise-medical-inc/903c1877-1140-4298-b4c8-565f68c374e7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 21, 2013
- [FDA Inspection 823440 - Inovise Medical, Inc. - 2013-03-21](https://www.globalkeysolutions.net/records/fda_inspections/inovise-medical-inc/b659e025-b32d-4447-bdcf-eb71871b835d) — classification: No Action Indicated (NAI), source: FDA, date: March 21, 2013
- [FDA Inspection 727390 - Inovise Medical, Inc. - 2011-06-01](https://www.globalkeysolutions.net/records/fda_inspections/inovise-medical-inc/e03768b4-4f80-4a21-a20d-bc84daefcbe7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 1, 2011
- [FDA Inspection 727390 - Inovise Medical, Inc. - 2011-06-01](https://www.globalkeysolutions.net/records/fda_inspections/inovise-medical-inc/a4c884a8-f145-4cb8-8e1d-92722d70c55d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 1, 2011

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