# FDA Inspection 1059220 - DermAvance Pharmaceuticals, Inc. - July 17, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/dermavance-pharmaceuticals-inc/aa82b371-b8b9-49ec-a1b7-9e2f1b51bdae
Source feed: FDA_Inspections

> FDA Inspection 1059220 for DermAvance Pharmaceuticals, Inc. on July 17, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059220
- Company Name: DermAvance Pharmaceuticals, Inc.
- Inspection Date: 2018-07-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/dermavance-pharmaceuticals-inc/fd276aaf-86f4-43f8-b96d-6a5b9515ea7b

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