FDA Inspection 1159190 — Infraredx, Inc.

Infraredx, Inc. — FEI 3015551113

The FDA completed an inspection of Infraredx, Inc. on December 8, 2021 in Bedford, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 8, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Bedford, MA (United States)