FDA Inspection 1071800 — Agnesian Healthcare IRB

Agnesian Healthcare IRB — FEI 3009793893

The FDA completed an inspection of Agnesian Healthcare IRB on November 5, 2018 in Fond Du Lac, WI. 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 5, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fond Du Lac, WI (United States)

Additional Details

IRB