FDA Inspection 861881 — Nytone Medical Products, Inc.
The FDA completed an inspection of Nytone Medical Products, Inc. on January 10, 2014 in Bluffdale, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- January 10, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Bluffdale, UT (United States)