FDA Inspection 959727 — Unisis Corp.

Unisis Corp. — FEI 3003803331

The FDA completed an inspection of Unisis Corp. on Feb 19, 2016 in Koshigaya. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 19, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Koshigaya (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.