FDA Inspection 1116325 — Unisis Corp.
The FDA completed an inspection of Unisis Corp. on January 23, 2020 in Koshigaya. 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
- January 23, 2020
- Fiscal Year
- 2020
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Koshigaya (Japan)