FDA Inspection 1074753 — InSitu Technologies, Inc.

InSitu Technologies, Inc. — FEI 3003407487

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

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