FDA Inspection 1057632 — Epiphany Cardiography Products
The FDA completed an inspection of Epiphany Cardiography Products on Apr 17, 2018 in Midlothian, VA. 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
- Apr 17, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Midlothian, VA (United States)