FDA Inspection 805650 — Welch Allyn, Inc.

Welch Allyn, Inc. — FEI 1316463

The FDA completed an inspection of Welch Allyn, Inc. on Oct 19, 2012 in Skaneateles Falls, NY. 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). Product area: Devices.