FDA Inspection 950339 — Nexus CMF, LLC
The FDA completed an inspection of Nexus CMF, LLC on Oct 1, 2015 in Cottonwood Heights, UT. 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). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 1, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Cottonwood Heights, UT (United States)