FDA Inspection 1157908 — Arjo, Inc.

Arjo, Inc. — FEI 1419652

The FDA completed an inspection of Arjo, Inc. on Dec 2, 2021 in hoffman estates, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 2, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
hoffman estates, IL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures