FDA Inspection 1059873 — Cutting Edge HC Brands

Cutting Edge HC Brands — FEI 3011285025

The FDA completed an inspection of Cutting Edge HC Brands on Jul 24, 2018 in Los Angeles, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 24, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Los Angeles, CA (United States)

Citations

IDCFRDescription
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures