FDA Inspection
Facemaster of Beverly Hills, Inc.Facemaster of Beverly Hills, Inc. – FDA Inspection, Feb 28, 2017
Record Details
This FDA Inspection record concerns Facemaster of Beverly Hills, Inc., with an inspection on February 28, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 58bb8b3a-3cda-473b-a9ad-351d1a0e6499
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1004520
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.100(b)Documentation
- 21 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
- 21 CFR 820.50(a)(3)Acceptable supplier records, inadequate records
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Facemaster of Beverly Hills, Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 20, 2025 | NAI | Los Angeles District Office | Postmarket Assurance: Medical Devices |
| September 18, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 18, 2013 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Facemaster of Beverly Hills, Inc.
- FDA Inspection 1279037 - 2025-08-20
- FDA Inspection 849833 - 2013-09-18
- FDA Inspection 849830 - 2013-09-18
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