FDA Inspection 1056044 — GE Medical Systems, LLC
The FDA completed an inspection of GE Medical Systems, LLC on Jun 14, 2018 in Waukesha, WI. 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)
- End Date
- Jun 14, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Waukesha, WI (United States)