FDA Inspection 938219 — Diasorin Inc.

Diasorin Inc. — FEI 2182595

The FDA completed an inspection of Diasorin Inc. on June 4, 2015 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
June 4, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Stillwater, MN (United States)