# FDA Inspection 924101 - Artisan Medical - May 04, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/artisan-medical/d9d604d3-8885-4477-9ce8-06422739fc6f
Source feed: FDA_Inspections

> FDA Inspection 924101 for Artisan Medical on May 04, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 924101
- Company Name: Artisan Medical
- Inspection Date: 2015-05-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1036785 - 2017-12-11](https://www.globalkeysolutions.net/records/fda_inspections/artisan-medical/0173fa7f-57fb-4b76-a2f0-49b513eb92d0)
- [FDA Inspection 1036785 - 2017-12-11](https://www.globalkeysolutions.net/records/fda_inspections/artisan-medical/0f76e182-35ab-467c-97fa-f0afd025b082)
- [FDA Inspection 924101 - 2015-05-04](https://www.globalkeysolutions.net/records/fda_inspections/artisan-medical/1b1588f0-3dc5-4829-923a-51a8c70826b4)

Company: https://www.globalkeysolutions.net/companies/artisan-medical/a293f832-5639-48a4-a306-6cf42cb87fa9

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7