FDA Inspection 1308272 — Elucid Bioimaging Inc.

Elucid Bioimaging Inc. — FEI 3013660213

The FDA completed an inspection of Elucid Bioimaging Inc. on March 20, 2026 in Boston, MA. 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
March 20, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Boston, MA (United States)

Citations

IDCFRDescription
23214ISO 13485:2016 Clause 8.2.2Complaint handling procedures not documented