FDA Inspection 1080275 — 1BYONE PRODUCTS INC
The FDA completed an inspection of 1BYONE PRODUCTS INC on Dec 11, 2018 in Ontario, 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). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 11, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Ontario, CA (United States)