# FDA Inspection 1036785 - Artisan Medical - December 11, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/artisan-medical/0173fa7f-57fb-4b76-a2f0-49b513eb92d0
Source feed: FDA_Inspections

> FDA Inspection 1036785 for Artisan Medical on December 11, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1036785
- Company Name: Artisan Medical
- Inspection Date: 2017-12-11
- Classification: No Action Indicated (NAI)
- 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/0f76e182-35ab-467c-97fa-f0afd025b082)
- [FDA Inspection 924101 - 2015-05-04](https://www.globalkeysolutions.net/records/fda_inspections/artisan-medical/d9d604d3-8885-4477-9ce8-06422739fc6f)
- [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