FDA Inspection 1061645 — Welch Allyn, Inc.

Welch Allyn, Inc. — FEI 1316463

The FDA completed an inspection of Welch Allyn, Inc. on Jul 19, 2018 in Skaneateles Falls, NY. 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
Jul 19, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Skaneateles Falls, NY (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.