FDA Inspection 1064412 — Wicab Inc

Wicab Inc — FEI 3005782280

The FDA completed an inspection of Wicab Inc on Aug 15, 2018 in Middleton, WI. 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
Aug 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Middleton, WI (United States)