# DERMACLIP US, LLC – FDA Inspection, Mar 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/dermaclip-us-llc/9fef8886-bb09-4412-bb69-6953755ab583
Source feed: FDA_Inspections

> FDA inspection 1020994 of DERMACLIP US, LLC, March 02, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020994
- Company Name: DERMACLIP US, LLC
- Inspection Date: 2017-03-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jocelyn-c-turner/7e39f6e0-9750-4460-8a4e-27ee9306b77e)

Company: https://www.keypedia.com/companies/dermaclip-us-llc/06e3f663-7d00-4a3d-9479-a9a97d1f64a8

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