FDA Inspection 935768 — Radiology Information Systems, Inc.
The FDA completed an inspection of Radiology Information Systems, Inc. on July 15, 2015 in Dulles, VA. 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
- July 15, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Dulles, VA (United States)