FDA Inspection 784308 — THEROZONE USA, INC.
The FDA completed an inspection of THEROZONE USA, INC. on May 31, 2012 in Santa Monica, CA. 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
- May 31, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Santa Monica, CA (United States)