# Ulthera Inc – FDA Inspection, Jul 26, 2018

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

> FDA inspection 1060604 of Ulthera Inc, July 26, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 10 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

Company: https://www.keypedia.com/companies/ulthera-inc/5b496f74-108b-4d0a-9a6f-67ebc92ecda6

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