FDA Inspection 1081144 — Diasorin Inc.

Diasorin Inc. — FEI 2182595

The FDA completed an inspection of Diasorin Inc. on February 1, 2019 in Stillwater, MN. 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
February 1, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Stillwater, MN (United States)

Additional Details

Sponsor, Contract Research Organization