FDA Inspection 890794 — Welch Allyn, Inc.

Welch Allyn, Inc. — FEI 1316463

The FDA completed an inspection of Welch Allyn, Inc. on August 13, 2014 in Skaneateles Falls, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 13, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Skaneateles Falls, NY (United States)

Citations

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