FDA Inspection 1074753 — InSitu Technologies, Inc.

InSitu Technologies, Inc. — FEI 3003407487

The FDA completed an inspection of InSitu Technologies, Inc. on November 20, 2018 in Saint Paul, 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
November 20, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)