FDA Inspection
Silhouette Lift, Inc.Silhouette Lift, Inc. – FDA Inspection, Jun 15, 2018
Record Details
This FDA Inspection record concerns Silhouette Lift, Inc., with an inspection on June 15, 2018, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · d5ad1e76-8209-4110-88a6-95d99b6a571d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1055876
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Silhouette Lift, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 5, 2014 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 22, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Silhouette Lift, Inc.
- FDA Inspection 902550 - 2014-11-05
- FDA Inspection 720613 - 2011-03-22
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.