# FDA Inspection 1060604 - Ulthera Inc - July 26, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/ulthera-inc/bf704cfb-cdfe-478b-b59c-bada010dcce2
Source feed: FDA_Inspections

> FDA Inspection 1060604 for Ulthera Inc on July 26, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060604
- Company Name: Ulthera Inc
- Inspection Date: 2018-07-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1060604 - 2018-07-26](https://www.globalkeysolutions.net/records/fda_inspections/ulthera-inc/6e646d0b-0d11-45aa-988a-b7044b69d5b8)
- [FDA Inspection 896887 - 2014-08-15](https://www.globalkeysolutions.net/records/fda_inspections/ulthera-inc/91aeb086-59c5-47c3-b301-8a275a0b7b83)
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Company: https://www.globalkeysolutions.net/companies/ulthera-inc/160c334b-0c06-432a-a7f8-a416c4b03314

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