FDA Inspection 1199005 — Amplion Clinical Communications, Inc.

Amplion Clinical Communications, Inc. — FEI 3009164985

The FDA completed an inspection of Amplion Clinical Communications, Inc. on February 16, 2023 in Nashville, TN. 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
February 16, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Nashville, TN (United States)

Citations

IDCFRDescription
73221 CFR 803.50(a)(2)Individual Report of Malfunction