FDA Inspection 987695 — Vida Diagnostics, Inc.

Vida Diagnostics, Inc. — FEI 3007233544

The FDA completed an inspection of Vida Diagnostics, Inc. on Oct 3, 2016 in Coralville, IA. 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
Oct 3, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Coralville, IA (United States)