FDA Inspection 1161187 — Landauer

Landauer — FEI 3008426232

The FDA completed an inspection of Landauer on Dec 16, 2021 in Glenwood, IL. 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
Dec 16, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Glenwood, IL (United States)