FDA Inspection 1164972 — Lucid Diagnostics, Inc.

Lucid Diagnostics, Inc. — FEI 3016490370

The FDA completed an inspection of Lucid Diagnostics, Inc. on Mar 21, 2022 in Foxboro, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 21, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Foxboro, MA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures