FDA Inspection 951025 — Alicia Diagnostics, Inc.

Alicia Diagnostics, Inc. — FEI 1000114012

The FDA completed an inspection of Alicia Diagnostics, Inc. on December 3, 2015 in Chuluota, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 3, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Chuluota, FL (United States)