# Silhouette Lift, Inc. – FDA Inspection, Jun 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/silhouette-lift-inc/d5ad1e76-8209-4110-88a6-95d99b6a571d
Source feed: FDA_Inspections

> FDA inspection 1055876 of Silhouette Lift, Inc., June 15, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055876
- Company Name: Silhouette Lift, Inc.
- Inspection Date: 2018-06-15
- 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 Documents

- [FDA Inspection 902550 - 2014-11-05](https://www.keypedia.com/records/fda_inspections/silhouette-lift-inc/41b5cecd-0e4b-41b4-b1ac-6555bba58986)
- FDA Inspection 720613 - 2011-03-22

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/silhouette-lift-inc/2278f805-bc8c-4e30-a206-5d4a72485314

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