FDA Inspection 1088818 — Emerge Diagnostics Inc.

Emerge Diagnostics Inc. — FEI 3009712031

The FDA completed an inspection of Emerge Diagnostics Inc. on April 26, 2019 in Carlsbad, CA. 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
April 26, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Carlsbad, CA (United States)