FDA Inspection 1025637 — Fenwal Inc

Fenwal Inc — FEI 3004548776

The FDA completed an inspection of Fenwal Inc on August 7, 2017 in Lake Zurich, IL. 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
August 7, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Lake Zurich, IL (United States)