FDA Inspection 1118136 — Retia Medical Systems Inc
The FDA completed an inspection of Retia Medical Systems Inc on December 2, 2019 in Valhalla, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- December 2, 2019
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Valhalla, NY (United States)