FDA Inspection
Beautyko LLCBeautyko LLC – FDA Inspection, Feb 14, 2013
Record Details
This FDA Inspection record concerns Beautyko LLC, with an inspection on February 14, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Beautyko LLC
- Inspection Date
- February 14, 2013
- Product Type
- Devices
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ID · 7fbc72c6-f6af-4d89-903e-ede0bc6309dc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 818707
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.198(a)Complaints
- 21 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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Other FDA inspections of Beautyko LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 14, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Beautyko LLC
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