FDA Inspection 1015213 — Hill-Rom, Inc.

Hill-Rom, Inc. — FEI 2027454

The FDA completed an inspection of Hill-Rom, Inc. on June 22, 2017 in Raleigh, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 22, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Raleigh, NC (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
332321 CFR 820.170(b)Installer records